ENST00000478003.2:n.2210T>A
|
|
|
ENST00000682276.1:n.1827T>A
|
|
|
ENST00000682892.1:c.1929T>A
|
ENSP00000507214.1:p.Pro643=
|
|
ENST00000682952.1:n.2021T>A
|
|
|
ENST00000684455.1:c.1595T>A
|
|
|
ENST00000684642.1:c.1779T>A
|
ENSP00000507355.1:p.Pro593=
|
|
ENST00000684740.1:n.2560T>A
|
|
|
ENST00000303236.9:c.2382T>A
MANE Select
|
ENSP00000307235.3:p.Pro794=
|
|
ENST00000652099.1:c.2576T>A
|
|
|
ENST00000652736.1:n.2258T>A
|
|
|
ENST00000303236.7:c.2382T>A
|
ENSP00000307235.3:p.Pro794=
|
|
ENST00000415570.1:c.2019T>A
|
ENSP00000412076.1:p.Pro673=
|
|
ENST00000419748.5:c.1929T>A
|
ENSP00000408325.1:p.Pro643=
|
|
ENST00000470706.1:n.49-24T>A
|
|
|
NM_001313915.1:c.1929T>A
|
NP_001300844.1:p.Pro643=
|
|
NM_004836.5:c.2382T>A
|
NP_004827.4:p.Pro794=
|
|
NM_004836.6:c.2382T>A
|
NP_004827.4:p.Pro794=
|
|
NR_110236.1:n.1238A>T
|
|
|
XM_005264649.3:c.1698T>A
|
XP_005264706.1:p.Pro566=
|
|
XM_017005376.2:c.1698T>A
|
XP_016860865.1:p.Pro566=
|
|
NM_004836.7:c.2382T>A
MANE Select
|
NP_004827.4:p.Pro794=
|
|
NM_001313915.2:c.1929T>A
|
NP_001300844.1:p.Pro643=
|
|