ENST00000556036.6:c.1520C>G
|
ENSP00000450596.1:p.Thr507Ser
|
|
ENST00000556250.6:c.1520C>G
|
ENSP00000452033.2:p.Thr507Ser
|
|
ENST00000696641.1:c.1361C>G
|
ENSP00000512774.1:p.Thr454Ser
|
|
ENST00000696642.1:c.*331C>G
|
ENSP00000512775.1:n.*331C>G
|
|
ENST00000696643.1:c.1520C>G
|
ENSP00000512776.1:p.Thr507Ser
|
|
ENST00000696646.1:c.*331C>G
|
ENSP00000512777.1:n.*331C>G
|
|
ENST00000696647.1:c.1520C>G
|
ENSP00000512778.1:p.Thr507Ser
|
|
ENST00000696648.1:c.1520C>G
|
ENSP00000512779.1:p.Thr507Ser
|
|
ENST00000696649.1:c.1520C>G
|
ENSP00000512780.1:p.Thr507Ser
|
|
ENST00000696650.1:n.1468C>G
|
|
|
ENST00000696658.1:n.2070C>G
|
|
|
ENST00000696662.1:c.1442C>G
|
ENSP00000512788.1:p.Thr481Ser
|
|
ENST00000696663.1:c.337C>G
|
|
|
ENST00000696664.1:c.337C>G
|
|
|
ENST00000696675.1:c.1520C>G
|
ENSP00000512799.1:p.Thr507Ser
|
|
ENST00000696680.1:c.1388C>G
|
ENSP00000512803.1:p.Thr463Ser
|
|
ENST00000696681.1:c.*331C>G
|
ENSP00000512804.1:n.*331C>G
|
|
ENST00000696682.1:c.1520C>G
|
ENSP00000512805.1:p.Thr507Ser
|
|
ENST00000696683.1:c.337C>G
|
|
|
ENST00000696684.1:c.337C>G
|
|
|
ENST00000696685.1:c.337C>G
|
|
|
ENST00000267430.10:c.1520C>G
MANE Select
|
ENSP00000267430.5:p.Thr507Ser
|
|
ENST00000267430.9:c.1520C>G
|
ENSP00000267430.5:p.Thr507Ser
|
|
ENST00000542564.6:c.1442C>G
|
ENSP00000442493.2:p.Thr481Ser
|
|
ENST00000556036.5:c.1520C>G
|
ENSP00000450596.1:p.Thr507Ser
|
|
ENST00000556250.5:c.275C>G
|
ENSP00000452033.1:p.Thr92Ser
|
|
NM_001308133.1:c.1442C>G
|
NP_001295062.1:p.Thr481Ser
|
|
NM_001308134.1:c.1520C>G
|
NP_001295063.1:p.Thr507Ser
|
|
NM_020937.2:c.1520C>G , LRG_502t1:c.1520C>G
|
NP_065988.1:p.Thr507Ser
|
|
NM_020937.3:c.1520C>G
|
NP_065988.1:p.Thr507Ser
|
|
XM_011537034.1:c.1520C>G
|
XP_011535336.1:p.Thr507Ser
|
|
XM_011537035.1:c.1442C>G
|
XP_011535337.1:p.Thr481Ser
|
|
XM_011537036.1:c.1520C>G
|
XP_011535338.1:p.Thr507Ser
|
|
XM_011537034.2:c.1520C>G
|
XP_011535336.1:p.Thr507Ser
|
|
XM_011537035.3:c.1442C>G
|
XP_011535337.1:p.Thr481Ser
|
|
XM_017021523.1:c.1520C>G
|
XP_016877012.1:p.Thr507Ser
|
|
XM_017021524.2:c.557C>G
|
XP_016877013.1:p.Thr186Ser
|
|
XM_017021525.2:c.335C>G
|
XP_016877014.1:p.Thr112Ser
|
|
XM_017021526.2:c.335C>G
|
XP_016877015.1:p.Thr112Ser
|
|
XM_017021527.1:c.335C>G
|
XP_016877016.1:p.Thr112Ser
|
|
XR_001750470.1:n.1612C>G
|
|
|
XR_001750471.2:n.1612C>G
|
|
|
XR_001750472.1:n.1612C>G
|
|
|
NM_020937.4:c.1520C>G
MANE Select
|
NP_065988.1:p.Thr507Ser
|
|
NM_001308133.2:c.1442C>G
|
NP_001295062.1:p.Thr481Ser
|
|
NM_001308134.2:c.1520C>G
|
NP_001295063.1:p.Thr507Ser
|
|