ENST00000695651.1:n.2547T>G
|
|
|
ENST00000695653.1:c.2108T>G
|
ENSP00000512084.1:p.Met703Arg
|
|
ENST00000695654.1:c.3224T>G
|
ENSP00000512085.1:p.Met1075Arg
|
|
ENST00000695689.1:c.170T>G
|
ENSP00000512101.1:n.170T>G
|
|
ENST00000695690.1:n.390T>G
|
|
|
ENST00000695691.1:n.390T>G
|
|
|
ENST00000245907.11:c.4199T>G
MANE Select
|
ENSP00000245907.4:p.Met1400Arg
|
|
ENST00000245907.10:c.4199T>G
|
ENSP00000245907.4:p.Met1400Arg
|
|
ENST00000596548.1:c.320T>G
|
ENSP00000469744.1:p.Met107Arg
|
|
ENST00000599899.5:n.1158T>G
|
|
|
ENST00000601008.1:c.242-4245T>G
|
ENSP00000471384.1:n.242-4245T>G
|
|
NM_000064.3:c.4199T>G
|
NP_000055.2:p.Met1400Arg
|
|
NM_000064.4:c.4199T>G
MANE Select
|
NP_000055.2:p.Met1400Arg
|
|