ENST00000478003.2:n.2248T=
|
|
|
ENST00000682276.1:n.1865T=
|
|
|
ENST00000682892.1:c.1967T=
|
ENSP00000507214.1:p.Val656=
|
|
ENST00000682952.1:n.2059T=
|
|
|
ENST00000684455.1:c.1633T=
|
|
|
ENST00000684642.1:c.1817T=
|
ENSP00000507355.1:p.Val606=
|
|
ENST00000684740.1:n.2598T=
|
|
|
ENST00000303236.9:c.2420T=
MANE Select
|
ENSP00000307235.3:p.Val807=
|
|
ENST00000652099.1:c.2614T=
|
|
|
ENST00000652736.1:n.2296T=
|
|
|
ENST00000303236.7:c.2420T=
|
ENSP00000307235.3:p.Val807=
|
|
ENST00000415570.1:c.2057T=
|
ENSP00000412076.1:p.Val686=
|
|
ENST00000419748.5:c.1967T=
|
ENSP00000408325.1:p.Val656=
|
|
ENST00000470706.1:n.63T=
|
|
|
NM_001313915.1:c.1967T=
|
NP_001300844.1:p.Val656=
|
|
NM_004836.5:c.2420T=
|
NP_004827.4:p.Val807=
|
|
NM_004836.6:c.2420T=
|
NP_004827.4:p.Val807=
|
|
NR_110236.1:n.1200A=
|
|
|
XM_005264649.3:c.1736T=
|
XP_005264706.1:p.Val579=
|
|
XM_017005376.2:c.1736T=
|
XP_016860865.1:p.Val579=
|
|
NM_004836.7:c.2420T=
MANE Select
|
NP_004827.4:p.Val807=
|
|
NM_001313915.2:c.1967T=
|
NP_001300844.1:p.Val656=
|
|