ENST00000350026.11:c.5013A>T
|
ENSP00000055163.8:p.Pro1671=
|
|
ENST00000414678.8:c.5082A>T
|
ENSP00000412835.3:p.Pro1694=
|
|
ENST00000637015.2:c.5301A>T
|
ENSP00000489729.2:p.Pro1767=
|
|
ENST00000346085.10:c.5052A>T
|
ENSP00000344546.5:p.Pro1684=
|
|
ENST00000350026.10:c.4764A>T
|
ENSP00000055163.7:p.Pro1588=
|
|
ENST00000414678.7:c.3330A>T
|
ENSP00000412835.2:p.Pro1110=
|
|
ENST00000635849.1:c.2493A>T
|
ENSP00000490948.1:p.Pro831=
|
|
ENST00000635957.1:c.2124A>T
|
ENSP00000490385.1:p.Pro708=
|
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ENST00000636227.1:n.3635A>T
|
|
|
ENST00000636254.1:n.1092A>T
|
|
|
ENST00000636930.2:c.5172A>T
MANE Select
|
ENSP00000490491.2:p.Pro1724=
|
|
ENST00000636940.1:n.3169A>T
|
|
|
ENST00000637015.1:c.2540A>T
|
|
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ENST00000637568.1:c.2454A>T
|
|
|
ENST00000637741.1:n.1838A>T
|
|
|
ENST00000637810.1:c.2514A>T
|
ENSP00000489636.1:p.Pro838=
|
|
ENST00000637904.1:c.2673A>T
|
ENSP00000490550.1:p.Pro891=
|
|
ENST00000647938.1:c.4803A>T
|
ENSP00000498155.1:p.Pro1601=
|
|
ENST00000346085.9:c.4803A>T
|
ENSP00000344546.4:p.Pro1601=
|
|
ENST00000350026.9:c.4764A>T
|
ENSP00000055163.7:p.Pro1588=
|
|
ENST00000414678.6:c.3330A>T
|
ENSP00000412835.2:p.Pro1110=
|
|
NM_017519.2:c.4764A>T
|
NP_059989.2:p.Pro1588=
|
|
NM_020732.3:c.4803A>T
|
NP_065783.3:p.Pro1601=
|
|
XM_005267069.3:c.4923A>T
|
XP_005267126.2:p.Pro1641=
|
|
XM_011535984.1:c.4002A>T
|
XP_011534286.1:p.Pro1334=
|
|
XM_011535985.1:c.3822A>T
|
XP_011534287.1:p.Pro1274=
|
|
XM_011535986.1:c.3582A>T
|
XP_011534288.1:p.Pro1194=
|
|
XM_011535987.1:c.3201A>T
|
XP_011534289.1:p.Pro1067=
|
|
XM_011535988.1:c.2064A>T
|
XP_011534290.1:p.Pro688=
|
|
NM_001346813.1:c.4923A>T
|
NP_001333742.1:p.Pro1641=
|
|
NM_001363725.1:c.2673A>T
|
NP_001350654.1:p.Pro891=
|
|
XM_011535984.2:c.5133A>T
|
XP_011534286.2:p.Pro1711=
|
|
XM_011535988.3:c.2064A>T
|
XP_011534290.1:p.Pro688=
|
|
XM_017011103.2:c.5034A>T
|
XP_016866592.1:p.Pro1678=
|
|
XM_017011104.1:c.5004A>T
|
XP_016866593.1:p.Pro1668=
|
|
XM_017011105.2:c.4974A>T
|
XP_016866594.1:p.Pro1658=
|
|
XM_017011106.2:c.4845A>T
|
XP_016866595.1:p.Pro1615=
|
|
XM_017011107.2:c.4824A>T
|
XP_016866596.1:p.Pro1608=
|
|
XR_002956289.1:n.5119A>T
|
|
|
NM_001363725.2:c.2673A>T
|
NP_001350654.1:p.Pro891=
|
|
NM_001371656.1:c.5052A>T
|
NP_001358585.1:p.Pro1684=
|
|
NM_001374820.1:c.5052A>T
|
NP_001361749.1:p.Pro1684=
|
|
NM_001374828.1:c.5172A>T
MANE Select
|
NP_001361757.1:p.Pro1724=
|
|
NM_017519.3:c.5013A>T
|
NP_059989.3:p.Pro1671=
|
|