ENST00000350026.11:c.4985T>G
|
ENSP00000055163.8:p.Val1662Gly
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ENST00000414678.8:c.5054T>G
|
ENSP00000412835.3:p.Val1685Gly
|
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ENST00000637015.2:c.5273T>G
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ENSP00000489729.2:p.Val1758Gly
|
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ENST00000346085.10:c.5024T>G
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ENSP00000344546.5:p.Val1675Gly
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ENST00000350026.10:c.4736T>G
|
ENSP00000055163.7:p.Val1579Gly
|
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ENST00000414678.7:c.3302T>G
|
ENSP00000412835.2:p.Val1101Gly
|
|
ENST00000635849.1:c.2465T>G
|
ENSP00000490948.1:p.Val822Gly
|
|
ENST00000635957.1:c.2096T>G
|
ENSP00000490385.1:p.Val699Gly
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ENST00000636227.1:n.3607T>G
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|
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ENST00000636254.1:n.1064T>G
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|
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ENST00000636930.2:c.5144T>G
MANE Select
|
ENSP00000490491.2:p.Val1715Gly
|
|
ENST00000636940.1:n.3141T>G
|
|
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ENST00000637015.1:c.2512T>G
|
|
|
ENST00000637568.1:c.2426T>G
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|
|
ENST00000637741.1:n.1810T>G
|
|
|
ENST00000637810.1:c.2486T>G
|
ENSP00000489636.1:p.Val829Gly
|
|
ENST00000637904.1:c.2645T>G
|
ENSP00000490550.1:p.Val882Gly
|
|
ENST00000647938.1:c.4775T>G
|
ENSP00000498155.1:p.Val1592Gly
|
|
ENST00000346085.9:c.4775T>G
|
ENSP00000344546.4:p.Val1592Gly
|
|
ENST00000350026.9:c.4736T>G
|
ENSP00000055163.7:p.Val1579Gly
|
|
ENST00000414678.6:c.3302T>G
|
ENSP00000412835.2:p.Val1101Gly
|
|
NM_017519.2:c.4736T>G
|
NP_059989.2:p.Val1579Gly
|
|
NM_020732.3:c.4775T>G
|
NP_065783.3:p.Val1592Gly
|
|
XM_005267069.3:c.4895T>G
|
XP_005267126.2:p.Val1632Gly
|
|
XM_011535984.1:c.3974T>G
|
XP_011534286.1:p.Val1325Gly
|
|
XM_011535985.1:c.3794T>G
|
XP_011534287.1:p.Val1265Gly
|
|
XM_011535986.1:c.3554T>G
|
XP_011534288.1:p.Val1185Gly
|
|
XM_011535987.1:c.3173T>G
|
XP_011534289.1:p.Val1058Gly
|
|
XM_011535988.1:c.2036T>G
|
XP_011534290.1:p.Val679Gly
|
|
NM_001346813.1:c.4895T>G
|
NP_001333742.1:p.Val1632Gly
|
|
NM_001363725.1:c.2645T>G
|
NP_001350654.1:p.Val882Gly
|
|
XM_011535984.2:c.5105T>G
|
XP_011534286.2:p.Val1702Gly
|
|
XM_011535988.3:c.2036T>G
|
XP_011534290.1:p.Val679Gly
|
|
XM_017011103.2:c.5006T>G
|
XP_016866592.1:p.Val1669Gly
|
|
XM_017011104.1:c.4976T>G
|
XP_016866593.1:p.Val1659Gly
|
|
XM_017011105.2:c.4946T>G
|
XP_016866594.1:p.Val1649Gly
|
|
XM_017011106.2:c.4817T>G
|
XP_016866595.1:p.Val1606Gly
|
|
XM_017011107.2:c.4796T>G
|
XP_016866596.1:p.Val1599Gly
|
|
XR_002956289.1:n.5091T>G
|
|
|
NM_001363725.2:c.2645T>G
|
NP_001350654.1:p.Val882Gly
|
|
NM_001371656.1:c.5024T>G
|
NP_001358585.1:p.Val1675Gly
|
|
NM_001374820.1:c.5024T>G
|
NP_001361749.1:p.Val1675Gly
|
|
NM_001374828.1:c.5144T>G
MANE Select
|
NP_001361757.1:p.Val1715Gly
|
|
NM_017519.3:c.4985T>G
|
NP_059989.3:p.Val1662Gly
|
|