ENST00000651671.1:c.6082G>A
MANE Select
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ENSP00000498587.1:p.Gly2028Ser
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ENST00000679595.1:c.*1122G>A
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ENSP00000506241.1:n.*1122G>A
|
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ENST00000679969.1:n.2563G>A
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ENST00000680003.1:n.2414G>A
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ENST00000680133.1:c.5968G>A
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ENSP00000505319.1:p.Gly1990Ser
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ENST00000680218.1:c.5962G>A
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ENSP00000505339.1:p.Gly1988Ser
|
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ENST00000680668.1:c.5968G>A
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ENSP00000506336.1:p.Gly1990Ser
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ENST00000680778.1:c.3679G>A
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ENSP00000506033.1:p.Gly1227Ser
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ENST00000680924.1:c.*3482G>A
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ENSP00000506031.1:n.*3482G>A
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ENST00000681135.1:c.*3691G>A
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ENSP00000506636.1:n.*3691G>A
|
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ENST00000681298.1:n.4187G>A
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ENST00000681454.1:c.*5318G>A
|
ENSP00000505763.1:n.*5318G>A
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ENST00000277541.6:c.6082G>A
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ENSP00000277541.6:p.Gly2028Ser
|
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NM_017617.3:c.6082G>A
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NP_060087.3:p.Gly2028Ser
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XM_011518717.1:c.5383G>A
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XP_011517019.1:p.Gly1795Ser
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NM_017617.5:c.6082G>A
MANE Select
|
NP_060087.3:p.Gly2028Ser
|
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XM_011518717.2:c.5359G>A
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XP_011517019.2:p.Gly1787Ser
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