ENST00000478003.2:n.1907A>T
|
|
|
ENST00000682276.1:n.1524A>T
|
|
|
ENST00000682892.1:c.1626A>T
|
ENSP00000507214.1:p.Pro542=
|
|
ENST00000682952.1:n.1718A>T
|
|
|
ENST00000684455.1:c.1292A>T
|
|
|
ENST00000684642.1:c.1476A>T
|
ENSP00000507355.1:p.Pro492=
|
|
ENST00000684740.1:n.2257A>T
|
|
|
ENST00000303236.9:c.2079A>T
MANE Select
|
ENSP00000307235.3:p.Pro693=
|
|
ENST00000652099.1:c.2273A>T
|
|
|
ENST00000652736.1:n.1955A>T
|
|
|
ENST00000303236.7:c.2079A>T
|
ENSP00000307235.3:p.Pro693=
|
|
ENST00000415570.1:c.1716A>T
|
ENSP00000412076.1:p.Pro572=
|
|
ENST00000419748.5:c.1626A>T
|
ENSP00000408325.1:p.Pro542=
|
|
ENST00000470706.1:n.5A>T
|
|
|
ENST00000478003.1:n.645A>T
|
|
|
NM_001313915.1:c.1626A>T
|
NP_001300844.1:p.Pro542=
|
|
NM_004836.5:c.2079A>T
|
NP_004827.4:p.Pro693=
|
|
NM_004836.6:c.2079A>T
|
NP_004827.4:p.Pro693=
|
|
NR_110236.1:n.1541T>A
|
|
|
XM_005264649.3:c.1395A>T
|
XP_005264706.1:p.Pro465=
|
|
XR_939749.1:n.2358A>T
|
|
|
XM_017005376.2:c.1395A>T
|
XP_016860865.1:p.Pro465=
|
|
NM_004836.7:c.2079A>T
MANE Select
|
NP_004827.4:p.Pro693=
|
|
NM_001313915.2:c.1626A>T
|
NP_001300844.1:p.Pro542=
|
|