ENST00000216075.11:c.814C>G
MANE Select
|
ENSP00000216075.6:p.Gln272Glu
|
|
ENST00000216075.10:c.814C>G
|
ENSP00000216075.6:p.Gln272Glu
|
|
ENST00000395732.7:c.800C>G
|
ENSP00000379081.3:p.Pro267Arg
|
|
ENST00000395733.7:c.683C>G
|
ENSP00000379082.3:p.Pro228Arg
|
|
ENST00000451761.1:c.754C>G
|
ENSP00000409894.1:p.Gln252Glu
|
|
NM_017584.5:c.814C>G
|
NP_060054.4:p.Gln272Glu
|
|
XM_005261925.3:c.676C>G
|
XP_005261982.1:p.Gln226Glu
|
|
XR_244455.2:n.3310C>G
|
|
|
XM_005261925.4:c.676C>G
|
XP_005261982.1:p.Gln226Glu
|
|
NM_017584.6:c.814C>G
MANE Select
|
NP_060054.4:p.Gln272Glu
|
|