ENST00000282479.8:c.761A>C
|
ENSP00000282479.6:p.Lys254Thr
|
|
ENST00000682752.1:c.*720A>C
|
ENSP00000507436.1:n.*720A>C
|
|
ENST00000682781.1:n.886A>C
|
|
|
ENST00000683764.1:n.1081A>C
|
|
|
ENST00000684240.1:n.972A>C
|
|
|
ENST00000684389.1:n.933A>C
|
|
|
ENST00000339673.11:c.809A>C
MANE Select
|
ENSP00000340935.6:p.Lys270Thr
|
|
ENST00000282479.7:c.761A>C
|
ENSP00000282479.6:p.Lys254Thr
|
|
ENST00000339673.10:c.809A>C
|
ENSP00000340935.6:p.Lys270Thr
|
|
NM_001079911.2:c.761A>C
|
NP_001073380.1:p.Lys254Thr
|
|
NM_004407.3:c.809A>C
|
NP_004398.1:p.Lys270Thr
|
|
XM_011531705.1:c.896A>C
|
XP_011530007.1:p.Lys299Thr
|
|
XM_011531706.1:c.848A>C
|
XP_011530008.1:p.Lys283Thr
|
|
XR_938960.1:n.115-5178T>G
|
|
|
XM_011531705.2:c.896A>C
|
XP_011530007.1:p.Lys299Thr
|
|
XM_011531706.2:c.848A>C
|
XP_011530008.1:p.Lys283Thr
|
|
XR_938960.2:n.115-5178T>G
|
|
|
NM_001079911.3:c.761A>C
|
NP_001073380.1:p.Lys254Thr
|
|
NM_004407.4:c.809A>C
MANE Select
|
NP_004398.1:p.Lys270Thr
|
|