ENST00000478003.2:n.1960T>G
|
|
|
ENST00000682276.1:n.1577T>G
|
|
|
ENST00000682892.1:c.1679T>G
|
ENSP00000507214.1:p.Ile560Ser
|
|
ENST00000682952.1:n.1771T>G
|
|
|
ENST00000684455.1:c.1345T>G
|
|
|
ENST00000684642.1:c.1529T>G
|
ENSP00000507355.1:p.Ile510Ser
|
|
ENST00000684740.1:n.2310T>G
|
|
|
ENST00000303236.9:c.2132T>G
MANE Select
|
ENSP00000307235.3:p.Ile711Ser
|
|
ENST00000652099.1:c.2326T>G
|
|
|
ENST00000652736.1:n.2008T>G
|
|
|
ENST00000303236.7:c.2132T>G
|
ENSP00000307235.3:p.Ile711Ser
|
|
ENST00000415570.1:c.1769T>G
|
ENSP00000412076.1:p.Ile590Ser
|
|
ENST00000419748.5:c.1679T>G
|
ENSP00000408325.1:p.Ile560Ser
|
|
ENST00000470706.1:n.48+10T>G
|
|
|
NM_001313915.1:c.1679T>G
|
NP_001300844.1:p.Ile560Ser
|
|
NM_004836.5:c.2132T>G
|
NP_004827.4:p.Ile711Ser
|
|
NM_004836.6:c.2132T>G
|
NP_004827.4:p.Ile711Ser
|
|
NR_110236.1:n.1488A>C
|
|
|
XM_005264649.3:c.1448T>G
|
XP_005264706.1:p.Ile483Ser
|
|
XR_939749.1:n.2411T>G
|
|
|
XM_017005376.2:c.1448T>G
|
XP_016860865.1:p.Ile483Ser
|
|
NM_004836.7:c.2132T>G
MANE Select
|
NP_004827.4:p.Ile711Ser
|
|
NM_001313915.2:c.1679T>G
|
NP_001300844.1:p.Ile560Ser
|
|