ENST00000478003.2:n.1969C>T
|
|
|
ENST00000682276.1:n.1586C>T
|
|
|
ENST00000682892.1:c.1688C>T
|
ENSP00000507214.1:p.Pro563Leu
|
|
ENST00000682952.1:n.1780C>T
|
|
|
ENST00000684455.1:c.1354C>T
|
|
|
ENST00000684642.1:c.1538C>T
|
ENSP00000507355.1:p.Pro513Leu
|
|
ENST00000684740.1:n.2319C>T
|
|
|
ENST00000303236.9:c.2141C>T
MANE Select
|
ENSP00000307235.3:p.Pro714Leu
|
|
ENST00000652099.1:c.2335C>T
|
|
|
ENST00000652736.1:n.2017C>T
|
|
|
ENST00000303236.7:c.2141C>T
|
ENSP00000307235.3:p.Pro714Leu
|
|
ENST00000415570.1:c.1778C>T
|
ENSP00000412076.1:p.Pro593Leu
|
|
ENST00000419748.5:c.1688C>T
|
ENSP00000408325.1:p.Pro563Leu
|
|
ENST00000470706.1:n.48+19C>T
|
|
|
NM_001313915.1:c.1688C>T
|
NP_001300844.1:p.Pro563Leu
|
|
NM_004836.5:c.2141C>T
|
NP_004827.4:p.Pro714Leu
|
|
NM_004836.6:c.2141C>T
|
NP_004827.4:p.Pro714Leu
|
|
NR_110236.1:n.1479G>A
|
|
|
XM_005264649.3:c.1457C>T
|
XP_005264706.1:p.Pro486Leu
|
|
XR_939749.1:n.2420C>T
|
|
|
XM_017005376.2:c.1457C>T
|
XP_016860865.1:p.Pro486Leu
|
|
NM_004836.7:c.2141C>T
MANE Select
|
NP_004827.4:p.Pro714Leu
|
|
NM_001313915.2:c.1688C>T
|
NP_001300844.1:p.Pro563Leu
|
|