ENST00000554809.6:c.2790T>G
|
ENSP00000450632.2:p.Val930=
|
|
ENST00000555484.2:c.356T>G
|
|
|
ENST00000556250.6:c.4371T>G
|
ENSP00000452033.2:p.Val1457=
|
|
ENST00000557110.2:c.356T>G
|
|
|
ENST00000696642.1:c.*3389T>G
|
ENSP00000512775.1:n.*3389T>G
|
|
ENST00000696644.1:n.314T>G
|
|
|
ENST00000696645.1:n.468T>G
|
|
|
ENST00000696647.1:c.4578T>G
|
ENSP00000512778.1:p.Val1526=
|
|
ENST00000696648.1:c.*2603T>G
|
ENSP00000512779.1:n.*2603T>G
|
|
ENST00000696649.1:c.4422T>G
|
ENSP00000512780.1:p.Val1474=
|
|
ENST00000696650.1:n.4526T>G
|
|
|
ENST00000696659.1:c.2576T>G
|
|
|
ENST00000696663.1:c.3509T>G
|
|
|
ENST00000696664.1:c.3410T>G
|
|
|
ENST00000696665.1:c.356T>G
|
|
|
ENST00000696675.1:c.*334T>G
|
ENSP00000512799.1:n.*334T>G
|
|
ENST00000696683.1:c.3395T>G
|
|
|
ENST00000696684.1:c.3395T>G
|
|
|
ENST00000696685.1:c.3395T>G
|
|
|
ENST00000696686.1:n.1315T>G
|
|
|
ENST00000267430.10:c.4578T>G
MANE Select
|
ENSP00000267430.5:p.Val1526=
|
|
ENST00000267430.9:c.4578T>G
|
ENSP00000267430.5:p.Val1526=
|
|
ENST00000542564.6:c.4500T>G
|
ENSP00000442493.2:p.Val1500=
|
|
ENST00000554809.5:c.1375T>G
|
|
|
ENST00000555013.1:n.411T>G
|
|
|
ENST00000556250.5:c.3126T>G
|
ENSP00000452033.1:p.Val1042=
|
|
NM_001308133.1:c.4500T>G
|
NP_001295062.1:p.Val1500=
|
|
NM_020937.2:c.4578T>G , LRG_502t1:c.4578T>G
|
NP_065988.1:p.Val1526=
|
|
NM_020937.3:c.4578T>G
|
NP_065988.1:p.Val1526=
|
|
XM_011537034.1:c.4593T>G
|
XP_011535336.1:p.Val1531=
|
|
XM_011537035.1:c.4515T>G
|
XP_011535337.1:p.Val1505=
|
|
XM_011537036.1:c.4593T>G
|
XP_011535338.1:p.Val1531=
|
|
XM_011537037.1:c.2607T>G
|
XP_011535339.1:p.Val869=
|
|
XM_011537034.2:c.4593T>G
|
XP_011535336.1:p.Val1531=
|
|
XM_011537035.3:c.4515T>G
|
XP_011535337.1:p.Val1505=
|
|
XM_011537037.3:c.2607T>G
|
XP_011535339.1:p.Val869=
|
|
XM_017021523.1:c.4593T>G
|
XP_016877012.1:p.Val1531=
|
|
XM_017021524.2:c.3630T>G
|
XP_016877013.1:p.Val1210=
|
|
XM_017021525.2:c.3408T>G
|
XP_016877014.1:p.Val1136=
|
|
XM_017021526.2:c.3408T>G
|
XP_016877015.1:p.Val1136=
|
|
XM_017021527.1:c.3393T>G
|
XP_016877016.1:p.Val1131=
|
|
XR_001750470.1:n.4685T>G
|
|
|
XR_001750471.2:n.4670T>G
|
|
|
XR_001750472.1:n.4722T>G
|
|
|
NM_020937.4:c.4578T>G
MANE Select
|
NP_065988.1:p.Val1526=
|
|
NM_001308133.2:c.4500T>G
|
NP_001295062.1:p.Val1500=
|
|