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ENSP00000496052.2:p.Tyr335=
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ENSP00000382840.3:p.Tyr290=
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ENSP00000414281.3:p.Tyr258=
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ENST00000457138.7:c.825C=
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ENSP00000392494.2:p.Tyr275=
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ENST00000629496.3:c.873C=
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ENSP00000487224.1:p.Tyr291=
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ENST00000631641.2:n.916C=
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ENST00000642161.1:n.3072C=
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ENST00000642322.1:c.315C=
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ENSP00000496052.1:p.Tyr105=
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ENST00000642424.1:c.315C=
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ENSP00000496356.1:p.Tyr105=
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ENST00000642589.1:n.4195C=
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ENST00000642597.1:n.1047C=
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ENST00000642687.1:n.906C=
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ENST00000642722.1:n.1706C=
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ENST00000642763.1:n.1764C=
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ENST00000642793.1:c.*322C=
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ENSP00000493976.1:n.*322C=
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ENST00000643820.1:n.149C=
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ENST00000643963.1:c.*155C=
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ENSP00000495264.1:n.*155C=
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ENST00000644073.1:c.831C=
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ENSP00000493475.1:p.Tyr277=
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ENST00000644074.1:c.870C=
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ENSP00000496663.1:p.Tyr290=
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ENST00000644109.1:c.870C=
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ENSP00000494952.1:p.Tyr290=
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ENST00000644307.1:n.964C=
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ENST00000644513.1:c.873C=
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ENST00000644677.1:c.756C=
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ENSP00000496524.1:p.Tyr252=
|
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ENST00000644876.2:c.873C=
MANE Select
|
ENSP00000494040.1:p.Tyr291=
|
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ENST00000644958.1:n.2534C=
|
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ENST00000645080.1:c.*2095C=
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ENST00000646107.1:c.756C=
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|
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|
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|
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|
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|
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|
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|
|
ENST00000646679.1:c.315C=
|
ENSP00000494887.1:p.Tyr105=
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ENST00000646822.1:n.1935C=
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ENST00000646940.1:n.1047C=
|
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ENST00000647286.1:n.971C=
|
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|
ENST00000399959.6:c.873C=
|
ENSP00000382840.2:p.Tyr291=
|
|
ENST00000441189.3:c.340+1697C=
|
ENSP00000414281.2:n.340+1697C=
|
|
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|
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|
|
ENST00000478993.5:c.873C=
|
ENSP00000478443.1:p.Tyr291=
|
|
ENST00000542215.5:n.921C=
|
|
|
ENST00000625837.2:c.873C=
|
ENSP00000486306.1:p.Tyr291=
|
|
ENST00000626301.2:c.873C=
|
ENSP00000486443.1:p.Tyr291=
|
|
ENST00000629496.2:c.873C=
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ENSP00000487224.1:p.Tyr291=
|
|
ENST00000629785.2:c.873C=
|
ENSP00000486516.1:p.Tyr291=
|
|
ENST00000630255.2:c.873C=
|
ENSP00000486720.1:p.Tyr291=
|
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ENST00000630370.2:c.873C=
|
ENSP00000487062.1:p.Tyr291=
|
|
ENST00000630858.2:c.873C=
|
ENSP00000486514.1:p.Tyr291=
|
|
NM_001193416.2:c.873C=
|
NP_001180345.1:p.Tyr291=
|
|
NM_001193417.2:c.825C=
|
NP_001180346.1:p.Tyr275=
|
|
NM_001356.4:c.873C=
|
NP_001347.3:p.Tyr291=
|
|
NR_126093.1:n.1818C=
|
|
|
XM_011543892.1:c.873C=
|
XP_011542194.1:p.Tyr291=
|
|
NM_001363819.1:c.315C=
|
NP_001350748.1:p.Tyr105=
|
|
XM_011543892.2:c.873C=
|
XP_011542194.1:p.Tyr291=
|
|
XM_017029313.1:c.315C=
|
XP_016884802.1:p.Tyr105=
|
|
NM_001193416.3:c.873C=
|
NP_001180345.1:p.Tyr291=
|
|
NM_001193417.3:c.825C=
|
NP_001180346.1:p.Tyr275=
|
|
NM_001356.5:c.873C=
MANE Select
|
NP_001347.3:p.Tyr291=
|
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