ENST00000282479.8:c.2T>G
|
ENSP00000282479.6:p.Met1Arg
|
|
ENST00000682752.1:c.2T>G
|
ENSP00000507436.1:p.Met1Arg
|
|
ENST00000682781.1:n.127T>G
|
|
|
ENST00000683764.1:n.165T>G
|
|
|
ENST00000684240.1:n.165T>G
|
|
|
ENST00000684389.1:n.126T>G
|
|
|
ENST00000339673.11:c.2T>G
MANE Select
|
ENSP00000340935.6:p.Met1Arg
|
|
ENST00000282479.7:c.2T>G
|
ENSP00000282479.6:p.Met1Arg
|
|
ENST00000339673.10:c.2T>G
|
ENSP00000340935.6:p.Met1Arg
|
|
NM_001079911.2:c.2T>G
|
NP_001073380.1:p.Met1Arg
|
|
NM_004407.3:c.2T>G
|
NP_004398.1:p.Met1Arg
|
|
XM_011531705.1:c.89T>G
|
XP_011530007.1:p.Met30Arg
|
|
XM_011531706.1:c.89T>G
|
XP_011530008.1:p.Met30Arg
|
|
XM_011531705.2:c.89T>G
|
XP_011530007.1:p.Met30Arg
|
|
XM_011531706.2:c.89T>G
|
XP_011530008.1:p.Met30Arg
|
|
NM_001079911.3:c.2T>G
|
NP_001073380.1:p.Met1Arg
|
|
NM_004407.4:c.2T>G
MANE Select
|
NP_004398.1:p.Met1Arg
|
|