ENST00000216075.11:c.*76A>G
MANE Select
|
ENSP00000216075.6:n.*76A>G
|
|
ENST00000216075.10:c.*76A>G
|
ENSP00000216075.6:n.*76A>G
|
|
ENST00000395732.7:c.*107A>G
|
ENSP00000379081.3:n.*107A>G
|
|
ENST00000395733.7:c.*107A>G
|
ENSP00000379082.3:n.*107A>G
|
|
ENST00000451761.1:c.874A>G
|
ENSP00000409894.1:n.874A>G
|
|
NM_017584.5:c.*76A>G
|
NP_060054.4:n.*76A>G
|
|
XM_005261925.3:c.*76A>G
|
XP_005261982.1:n.*76A>G
|
|
XR_244455.2:n.3430A>G
|
|
|
XM_005261925.4:c.*76A>G
|
XP_005261982.1:n.*76A>G
|
|
NM_017584.6:c.*76A>G
MANE Select
|
NP_060054.4:n.*76A>G
|
|