ENST00000282479.8:c.1340A>G
|
ENSP00000282479.6:p.Lys447Arg
|
|
ENST00000682752.1:c.*1299A>G
|
ENSP00000507436.1:n.*1299A>G
|
|
ENST00000682781.1:n.1465A>G
|
|
|
ENST00000683764.1:n.1660A>G
|
|
|
ENST00000684240.1:n.1551A>G
|
|
|
ENST00000684389.1:n.1512A>G
|
|
|
ENST00000339673.11:c.1388A>G
MANE Select
|
ENSP00000340935.6:p.Lys463Arg
|
|
ENST00000282479.7:c.1340A>G
|
ENSP00000282479.6:p.Lys447Arg
|
|
ENST00000339673.10:c.1388A>G
|
ENSP00000340935.6:p.Lys463Arg
|
|
NM_001079911.2:c.1340A>G
|
NP_001073380.1:p.Lys447Arg
|
|
NM_004407.3:c.1388A>G
|
NP_004398.1:p.Lys463Arg
|
|
XM_011531705.1:c.1475A>G
|
XP_011530007.1:p.Lys492Arg
|
|
XM_011531706.1:c.1427A>G
|
XP_011530008.1:p.Lys476Arg
|
|
XR_938960.1:n.115-5757T>C
|
|
|
XM_011531705.2:c.1475A>G
|
XP_011530007.1:p.Lys492Arg
|
|
XM_011531706.2:c.1427A>G
|
XP_011530008.1:p.Lys476Arg
|
|
XR_938960.2:n.115-5757T>C
|
|
|
NM_001079911.3:c.1340A>G
|
NP_001073380.1:p.Lys447Arg
|
|
NM_004407.4:c.1388A>G
MANE Select
|
NP_004398.1:p.Lys463Arg
|
|