ENST00000322776.11:c.1157G=
MANE Select
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ENSP00000322450.6:p.Arg386=
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ENST00000647561.1:c.1157G=
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ENSP00000497587.1:p.Arg386=
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|
ENST00000322776.10:c.1157G=
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ENSP00000322450.6:p.Arg386=
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|
ENST00000415352.6:c.1136G=
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ENSP00000395368.2:p.Arg379=
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ENST00000526770.5:n.1440G=
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|
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ENST00000527355.5:c.370-147G=
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ENSP00000432637.1:n.370-147G=
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ENST00000527923.1:n.499G=
|
|
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ENST00000529927.5:c.1130G=
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ENSP00000436766.1:p.Arg377=
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|
ENST00000531250.1:n.421G=
|
|
|
ENST00000532303.5:c.854G=
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ENSP00000432015.1:p.Arg285=
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|
ENST00000533919.5:c.561G=
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ENSP00000435199.1:n.561G=
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|
ENST00000534352.1:n.255G=
|
|
|
NM_001166102.1:c.1130G=
|
NP_001159574.1:p.Arg377=
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|
NM_007103.3:c.1157G=
|
NP_009034.2:p.Arg386=
|
|
NM_001166102.2:c.1130G=
|
NP_001159574.1:p.Arg377=
|
|
NM_007103.4:c.1157G=
MANE Select
|
NP_009034.2:p.Arg386=
|
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