ENST00000490576.2:c.-1-183T=
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ENSP00000478839.2:n.-1-183T=
|
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ENST00000610745.5:c.-1-183T=
MANE Select
|
ENSP00000478561.1:n.-1-183T=
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ENST00000490576.1:c.-1-183T=
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ENSP00000478839.1:n.-1-183T=
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ENST00000494864.1:c.-70-4262T=
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ENSP00000479876.1:n.-70-4262T=
|
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ENST00000610745.4:c.-1-183T=
|
ENSP00000478561.1:n.-1-183T=
|
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ENST00000613082.1:n.375+208T=
|
|
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ENST00000614273.1:c.-1-183T=
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ENSP00000483678.1:n.-1-183T=
|
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NM_000104.3:c.-1-183T=
|
NP_000095.2:n.-1-183T=
|
|
XM_011533236.1:c.186A=
|
XP_011531538.1:p.Arg62=
|
|
NM_000104.4:c.-1-183T=
MANE Select
|
NP_000095.2:n.-1-183T=
|
|