ENST00000350026.11:c.5010C>G
|
ENSP00000055163.8:p.Pro1670=
|
|
ENST00000414678.8:c.5079C>G
|
ENSP00000412835.3:p.Pro1693=
|
|
ENST00000637015.2:c.5298C>G
|
ENSP00000489729.2:p.Pro1766=
|
|
ENST00000346085.10:c.5049C>G
|
ENSP00000344546.5:p.Pro1683=
|
|
ENST00000350026.10:c.4761C>G
|
ENSP00000055163.7:p.Pro1587=
|
|
ENST00000414678.7:c.3327C>G
|
ENSP00000412835.2:p.Pro1109=
|
|
ENST00000635849.1:c.2490C>G
|
ENSP00000490948.1:p.Pro830=
|
|
ENST00000635957.1:c.2121C>G
|
ENSP00000490385.1:p.Pro707=
|
|
ENST00000636227.1:n.3632C>G
|
|
|
ENST00000636254.1:n.1089C>G
|
|
|
ENST00000636930.2:c.5169C>G
MANE Select
|
ENSP00000490491.2:p.Pro1723=
|
|
ENST00000636940.1:n.3166C>G
|
|
|
ENST00000637015.1:c.2537C>G
|
|
|
ENST00000637568.1:c.2451C>G
|
|
|
ENST00000637741.1:n.1835C>G
|
|
|
ENST00000637810.1:c.2511C>G
|
ENSP00000489636.1:p.Pro837=
|
|
ENST00000637904.1:c.2670C>G
|
ENSP00000490550.1:p.Pro890=
|
|
ENST00000647938.1:c.4800C>G
|
ENSP00000498155.1:p.Pro1600=
|
|
ENST00000346085.9:c.4800C>G
|
ENSP00000344546.4:p.Pro1600=
|
|
ENST00000350026.9:c.4761C>G
|
ENSP00000055163.7:p.Pro1587=
|
|
ENST00000414678.6:c.3327C>G
|
ENSP00000412835.2:p.Pro1109=
|
|
NM_017519.2:c.4761C>G
|
NP_059989.2:p.Pro1587=
|
|
NM_020732.3:c.4800C>G
|
NP_065783.3:p.Pro1600=
|
|
XM_005267069.3:c.4920C>G
|
XP_005267126.2:p.Pro1640=
|
|
XM_011535984.1:c.3999C>G
|
XP_011534286.1:p.Pro1333=
|
|
XM_011535985.1:c.3819C>G
|
XP_011534287.1:p.Pro1273=
|
|
XM_011535986.1:c.3579C>G
|
XP_011534288.1:p.Pro1193=
|
|
XM_011535987.1:c.3198C>G
|
XP_011534289.1:p.Pro1066=
|
|
XM_011535988.1:c.2061C>G
|
XP_011534290.1:p.Pro687=
|
|
NM_001346813.1:c.4920C>G
|
NP_001333742.1:p.Pro1640=
|
|
NM_001363725.1:c.2670C>G
|
NP_001350654.1:p.Pro890=
|
|
XM_011535984.2:c.5130C>G
|
XP_011534286.2:p.Pro1710=
|
|
XM_011535988.3:c.2061C>G
|
XP_011534290.1:p.Pro687=
|
|
XM_017011103.2:c.5031C>G
|
XP_016866592.1:p.Pro1677=
|
|
XM_017011104.1:c.5001C>G
|
XP_016866593.1:p.Pro1667=
|
|
XM_017011105.2:c.4971C>G
|
XP_016866594.1:p.Pro1657=
|
|
XM_017011106.2:c.4842C>G
|
XP_016866595.1:p.Pro1614=
|
|
XM_017011107.2:c.4821C>G
|
XP_016866596.1:p.Pro1607=
|
|
XR_002956289.1:n.5116C>G
|
|
|
NM_001363725.2:c.2670C>G
|
NP_001350654.1:p.Pro890=
|
|
NM_001371656.1:c.5049C>G
|
NP_001358585.1:p.Pro1683=
|
|
NM_001374820.1:c.5049C>G
|
NP_001361749.1:p.Pro1683=
|
|
NM_001374828.1:c.5169C>G
MANE Select
|
NP_001361757.1:p.Pro1723=
|
|
NM_017519.3:c.5010C>G
|
NP_059989.3:p.Pro1670=
|
|