ENST00000554809.6:c.2795C>G
|
ENSP00000450632.2:p.Ser932Ter
|
|
ENST00000555484.2:c.361C>G
|
|
|
ENST00000556250.6:c.4376C>G
|
ENSP00000452033.2:p.Ser1459Ter
|
|
ENST00000557110.2:c.361C>G
|
|
|
ENST00000696642.1:c.*3394C>G
|
ENSP00000512775.1:n.*3394C>G
|
|
ENST00000696644.1:n.319C>G
|
|
|
ENST00000696645.1:n.473C>G
|
|
|
ENST00000696647.1:c.4583C>G
|
ENSP00000512778.1:p.Ser1528Ter
|
|
ENST00000696648.1:c.*2608C>G
|
ENSP00000512779.1:n.*2608C>G
|
|
ENST00000696649.1:c.4427C>G
|
ENSP00000512780.1:p.Ser1476Ter
|
|
ENST00000696650.1:n.4531C>G
|
|
|
ENST00000696659.1:c.2581C>G
|
|
|
ENST00000696663.1:c.3514C>G
|
|
|
ENST00000696664.1:c.3415C>G
|
|
|
ENST00000696665.1:c.361C>G
|
|
|
ENST00000696675.1:c.*339C>G
|
ENSP00000512799.1:n.*339C>G
|
|
ENST00000696683.1:c.3400C>G
|
|
|
ENST00000696684.1:c.3400C>G
|
|
|
ENST00000696685.1:c.3400C>G
|
|
|
ENST00000696686.1:n.1320C>G
|
|
|
ENST00000267430.10:c.4583C>G
MANE Select
|
ENSP00000267430.5:p.Ser1528Ter
|
|
ENST00000267430.9:c.4583C>G
|
ENSP00000267430.5:p.Ser1528Ter
|
|
ENST00000542564.6:c.4505C>G
|
ENSP00000442493.2:p.Ser1502Ter
|
|
ENST00000554809.5:c.1380C>G
|
|
|
ENST00000555013.1:n.416C>G
|
|
|
ENST00000556250.5:c.3131C>G
|
ENSP00000452033.1:p.Ser1044Ter
|
|
NM_001308133.1:c.4505C>G
|
NP_001295062.1:p.Ser1502Ter
|
|
NM_020937.2:c.4583C>G , LRG_502t1:c.4583C>G
|
NP_065988.1:p.Ser1528Ter
|
|
NM_020937.3:c.4583C>G
|
NP_065988.1:p.Ser1528Ter
|
|
XM_011537034.1:c.4598C>G
|
XP_011535336.1:p.Ser1533Ter
|
|
XM_011537035.1:c.4520C>G
|
XP_011535337.1:p.Ser1507Ter
|
|
XM_011537036.1:c.4598C>G
|
XP_011535338.1:p.Ser1533Ter
|
|
XM_011537037.1:c.2612C>G
|
XP_011535339.1:p.Ser871Ter
|
|
XM_011537034.2:c.4598C>G
|
XP_011535336.1:p.Ser1533Ter
|
|
XM_011537035.3:c.4520C>G
|
XP_011535337.1:p.Ser1507Ter
|
|
XM_011537037.3:c.2612C>G
|
XP_011535339.1:p.Ser871Ter
|
|
XM_017021523.1:c.4598C>G
|
XP_016877012.1:p.Ser1533Ter
|
|
XM_017021524.2:c.3635C>G
|
XP_016877013.1:p.Ser1212Ter
|
|
XM_017021525.2:c.3413C>G
|
XP_016877014.1:p.Ser1138Ter
|
|
XM_017021526.2:c.3413C>G
|
XP_016877015.1:p.Ser1138Ter
|
|
XM_017021527.1:c.3398C>G
|
XP_016877016.1:p.Ser1133Ter
|
|
XR_001750470.1:n.4690C>G
|
|
|
XR_001750471.2:n.4675C>G
|
|
|
XR_001750472.1:n.4727C>G
|
|
|
NM_020937.4:c.4583C>G
MANE Select
|
NP_065988.1:p.Ser1528Ter
|
|
NM_001308133.2:c.4505C>G
|
NP_001295062.1:p.Ser1502Ter
|
|