ENST00000554809.6:c.2835A=
|
ENSP00000450632.2:p.Ser945=
|
|
ENST00000555484.2:c.401A=
|
|
|
ENST00000556250.6:c.4416A=
|
ENSP00000452033.2:p.Ser1472=
|
|
ENST00000557110.2:c.401A=
|
|
|
ENST00000696642.1:c.*3434A=
|
ENSP00000512775.1:n.*3434A=
|
|
ENST00000696644.1:n.359A=
|
|
|
ENST00000696645.1:n.513A=
|
|
|
ENST00000696647.1:c.4623A=
|
ENSP00000512778.1:p.Ser1541=
|
|
ENST00000696648.1:c.*2648A=
|
ENSP00000512779.1:n.*2648A=
|
|
ENST00000696649.1:c.4467A=
|
ENSP00000512780.1:p.Ser1489=
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ENST00000696650.1:n.4571A=
|
|
|
ENST00000696659.1:c.2621A=
|
|
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ENST00000696663.1:c.3554A=
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ENST00000696664.1:c.3455A=
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|
|
ENST00000696665.1:c.401A=
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|
|
ENST00000696675.1:c.*379A=
|
ENSP00000512799.1:n.*379A=
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|
ENST00000696683.1:c.3440A=
|
|
|
ENST00000696684.1:c.3440A=
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ENST00000696685.1:c.3440A=
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|
|
ENST00000696686.1:n.1360A=
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|
|
ENST00000267430.10:c.4623A=
MANE Select
|
ENSP00000267430.5:p.Ser1541=
|
|
ENST00000267430.9:c.4623A=
|
ENSP00000267430.5:p.Ser1541=
|
|
ENST00000542564.6:c.4545A=
|
ENSP00000442493.2:p.Ser1515=
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|
ENST00000554809.5:c.1420A=
|
|
|
ENST00000555013.1:n.456A=
|
|
|
ENST00000556250.5:c.3171A=
|
ENSP00000452033.1:p.Ser1057=
|
|
NM_001308133.1:c.4545A=
|
NP_001295062.1:p.Ser1515=
|
|
NM_020937.2:c.4623A= , LRG_502t1:c.4623A=
|
NP_065988.1:p.Ser1541=
|
|
NM_020937.3:c.4623A=
|
NP_065988.1:p.Ser1541=
|
|
XM_011537034.1:c.4638A=
|
XP_011535336.1:p.Ser1546=
|
|
XM_011537035.1:c.4560A=
|
XP_011535337.1:p.Ser1520=
|
|
XM_011537036.1:c.4638A=
|
XP_011535338.1:p.Ser1546=
|
|
XM_011537037.1:c.2652A=
|
XP_011535339.1:p.Ser884=
|
|
XM_011537034.2:c.4638A=
|
XP_011535336.1:p.Ser1546=
|
|
XM_011537035.3:c.4560A=
|
XP_011535337.1:p.Ser1520=
|
|
XM_011537037.3:c.2652A=
|
XP_011535339.1:p.Ser884=
|
|
XM_017021523.1:c.4638A=
|
XP_016877012.1:p.Ser1546=
|
|
XM_017021524.2:c.3675A=
|
XP_016877013.1:p.Ser1225=
|
|
XM_017021525.2:c.3453A=
|
XP_016877014.1:p.Ser1151=
|
|
XM_017021526.2:c.3453A=
|
XP_016877015.1:p.Ser1151=
|
|
XM_017021527.1:c.3438A=
|
XP_016877016.1:p.Ser1146=
|
|
XR_001750470.1:n.4730A=
|
|
|
XR_001750471.2:n.4715A=
|
|
|
XR_001750472.1:n.4767A=
|
|
|
NM_020937.4:c.4623A=
MANE Select
|
NP_065988.1:p.Ser1541=
|
|
NM_001308133.2:c.4545A=
|
NP_001295062.1:p.Ser1515=
|
|