ENST00000554809.6:c.2831C>T
|
ENSP00000450632.2:p.Ser944Phe
|
|
ENST00000555484.2:c.397C>T
|
|
|
ENST00000556250.6:c.4412C>T
|
ENSP00000452033.2:p.Ser1471Phe
|
|
ENST00000557110.2:c.397C>T
|
|
|
ENST00000696642.1:c.*3430C>T
|
ENSP00000512775.1:n.*3430C>T
|
|
ENST00000696644.1:n.355C>T
|
|
|
ENST00000696645.1:n.509C>T
|
|
|
ENST00000696647.1:c.4619C>T
|
ENSP00000512778.1:p.Ser1540Phe
|
|
ENST00000696648.1:c.*2644C>T
|
ENSP00000512779.1:n.*2644C>T
|
|
ENST00000696649.1:c.4463C>T
|
ENSP00000512780.1:p.Ser1488Phe
|
|
ENST00000696650.1:n.4567C>T
|
|
|
ENST00000696659.1:c.2617C>T
|
|
|
ENST00000696663.1:c.3550C>T
|
|
|
ENST00000696664.1:c.3451C>T
|
|
|
ENST00000696665.1:c.397C>T
|
|
|
ENST00000696675.1:c.*375C>T
|
ENSP00000512799.1:n.*375C>T
|
|
ENST00000696683.1:c.3436C>T
|
|
|
ENST00000696684.1:c.3436C>T
|
|
|
ENST00000696685.1:c.3436C>T
|
|
|
ENST00000696686.1:n.1356C>T
|
|
|
ENST00000267430.10:c.4619C>T
MANE Select
|
ENSP00000267430.5:p.Ser1540Phe
|
|
ENST00000267430.9:c.4619C>T
|
ENSP00000267430.5:p.Ser1540Phe
|
|
ENST00000542564.6:c.4541C>T
|
ENSP00000442493.2:p.Ser1514Phe
|
|
ENST00000554809.5:c.1416C>T
|
|
|
ENST00000555013.1:n.452C>T
|
|
|
ENST00000556250.5:c.3167C>T
|
ENSP00000452033.1:p.Ser1056Phe
|
|
NM_001308133.1:c.4541C>T
|
NP_001295062.1:p.Ser1514Phe
|
|
NM_020937.2:c.4619C>T , LRG_502t1:c.4619C>T
|
NP_065988.1:p.Ser1540Phe
|
|
NM_020937.3:c.4619C>T
|
NP_065988.1:p.Ser1540Phe
|
|
XM_011537034.1:c.4634C>T
|
XP_011535336.1:p.Ser1545Phe
|
|
XM_011537035.1:c.4556C>T
|
XP_011535337.1:p.Ser1519Phe
|
|
XM_011537036.1:c.4634C>T
|
XP_011535338.1:p.Ser1545Phe
|
|
XM_011537037.1:c.2648C>T
|
XP_011535339.1:p.Ser883Phe
|
|
XM_011537034.2:c.4634C>T
|
XP_011535336.1:p.Ser1545Phe
|
|
XM_011537035.3:c.4556C>T
|
XP_011535337.1:p.Ser1519Phe
|
|
XM_011537037.3:c.2648C>T
|
XP_011535339.1:p.Ser883Phe
|
|
XM_017021523.1:c.4634C>T
|
XP_016877012.1:p.Ser1545Phe
|
|
XM_017021524.2:c.3671C>T
|
XP_016877013.1:p.Ser1224Phe
|
|
XM_017021525.2:c.3449C>T
|
XP_016877014.1:p.Ser1150Phe
|
|
XM_017021526.2:c.3449C>T
|
XP_016877015.1:p.Ser1150Phe
|
|
XM_017021527.1:c.3434C>T
|
XP_016877016.1:p.Ser1145Phe
|
|
XR_001750470.1:n.4726C>T
|
|
|
XR_001750471.2:n.4711C>T
|
|
|
XR_001750472.1:n.4763C>T
|
|
|
NM_020937.4:c.4619C>T
MANE Select
|
NP_065988.1:p.Ser1540Phe
|
|
NM_001308133.2:c.4541C>T
|
NP_001295062.1:p.Ser1514Phe
|
|