ENST00000478003.2:n.2215T>A
|
|
|
ENST00000682276.1:n.1832T>A
|
|
|
ENST00000682892.1:c.1934T>A
|
ENSP00000507214.1:p.Val645Glu
|
|
ENST00000682952.1:n.2026T>A
|
|
|
ENST00000684455.1:c.1600T>A
|
|
|
ENST00000684642.1:c.1784T>A
|
ENSP00000507355.1:p.Val595Glu
|
|
ENST00000684740.1:n.2565T>A
|
|
|
ENST00000303236.9:c.2387T>A
MANE Select
|
ENSP00000307235.3:p.Val796Glu
|
|
ENST00000652099.1:c.2581T>A
|
|
|
ENST00000652736.1:n.2263T>A
|
|
|
ENST00000303236.7:c.2387T>A
|
ENSP00000307235.3:p.Val796Glu
|
|
ENST00000415570.1:c.2024T>A
|
ENSP00000412076.1:p.Val675Glu
|
|
ENST00000419748.5:c.1934T>A
|
ENSP00000408325.1:p.Val645Glu
|
|
ENST00000470706.1:n.49-19T>A
|
|
|
NM_001313915.1:c.1934T>A
|
NP_001300844.1:p.Val645Glu
|
|
NM_004836.5:c.2387T>A
|
NP_004827.4:p.Val796Glu
|
|
NM_004836.6:c.2387T>A
|
NP_004827.4:p.Val796Glu
|
|
NR_110236.1:n.1233A>T
|
|
|
XM_005264649.3:c.1703T>A
|
XP_005264706.1:p.Val568Glu
|
|
XM_017005376.2:c.1703T>A
|
XP_016860865.1:p.Val568Glu
|
|
NM_004836.7:c.2387T>A
MANE Select
|
NP_004827.4:p.Val796Glu
|
|
NM_001313915.2:c.1934T>A
|
NP_001300844.1:p.Val645Glu
|
|