ENST00000703783.1:n.608T>G
|
|
|
ENST00000703785.1:n.689T>G
|
|
|
ENST00000262464.9:c.3824T>G
MANE Select
|
ENSP00000262464.4:p.Met1275Arg
|
|
ENST00000262464.8:c.3824T>G
|
ENSP00000262464.4:p.Met1275Arg
|
|
ENST00000507835.5:c.374T>G
|
ENSP00000426839.1:p.Met125Arg
|
|
ENST00000508053.5:c.3824T>G
|
ENSP00000424571.1:p.Met1275Arg
|
|
ENST00000508989.5:c.3725T>G
|
ENSP00000425596.1:p.Met1242Arg
|
|
ENST00000619499.4:c.3821T>G
|
ENSP00000482132.1:p.Met1274Arg
|
|
NM_001999.3:c.3824T>G
|
NP_001990.2:p.Met1275Arg
|
|
XM_017009228.2:c.3671T>G
|
XP_016864717.1:p.Met1224Arg
|
|
NM_001999.4:c.3824T>G
MANE Select
|
NP_001990.2:p.Met1275Arg
|
|