ENST00000216075.11:c.813C>T
MANE Select
|
ENSP00000216075.6:p.Tyr271=
|
|
ENST00000216075.10:c.813C>T
|
ENSP00000216075.6:p.Tyr271=
|
|
ENST00000395732.7:c.799C>T
|
ENSP00000379081.3:p.Pro267Ser
|
|
ENST00000395733.7:c.682C>T
|
ENSP00000379082.3:p.Pro228Ser
|
|
ENST00000451761.1:c.753C>T
|
ENSP00000409894.1:p.Tyr251=
|
|
NM_017584.5:c.813C>T
|
NP_060054.4:p.Tyr271=
|
|
XM_005261925.3:c.675C>T
|
XP_005261982.1:p.Tyr225=
|
|
XR_244455.2:n.3309C>T
|
|
|
XM_005261925.4:c.675C>T
|
XP_005261982.1:p.Tyr225=
|
|
NM_017584.6:c.813C>T
MANE Select
|
NP_060054.4:p.Tyr271=
|
|