ENST00000350026.11:c.4999C>G
|
ENSP00000055163.8:p.Pro1667Ala
|
|
ENST00000414678.8:c.5068C>G
|
ENSP00000412835.3:p.Pro1690Ala
|
|
ENST00000637015.2:c.5287C>G
|
ENSP00000489729.2:p.Pro1763Ala
|
|
ENST00000346085.10:c.5038C>G
|
ENSP00000344546.5:p.Pro1680Ala
|
|
ENST00000350026.10:c.4750C>G
|
ENSP00000055163.7:p.Pro1584Ala
|
|
ENST00000414678.7:c.3316C>G
|
ENSP00000412835.2:p.Pro1106Ala
|
|
ENST00000635849.1:c.2479C>G
|
ENSP00000490948.1:p.Pro827Ala
|
|
ENST00000635957.1:c.2110C>G
|
ENSP00000490385.1:p.Pro704Ala
|
|
ENST00000636227.1:n.3621C>G
|
|
|
ENST00000636254.1:n.1078C>G
|
|
|
ENST00000636930.2:c.5158C>G
MANE Select
|
ENSP00000490491.2:p.Pro1720Ala
|
|
ENST00000636940.1:n.3155C>G
|
|
|
ENST00000637015.1:c.2526C>G
|
|
|
ENST00000637568.1:c.2440C>G
|
|
|
ENST00000637741.1:n.1824C>G
|
|
|
ENST00000637810.1:c.2500C>G
|
ENSP00000489636.1:p.Pro834Ala
|
|
ENST00000637904.1:c.2659C>G
|
ENSP00000490550.1:p.Pro887Ala
|
|
ENST00000647938.1:c.4789C>G
|
ENSP00000498155.1:p.Pro1597Ala
|
|
ENST00000346085.9:c.4789C>G
|
ENSP00000344546.4:p.Pro1597Ala
|
|
ENST00000350026.9:c.4750C>G
|
ENSP00000055163.7:p.Pro1584Ala
|
|
ENST00000414678.6:c.3316C>G
|
ENSP00000412835.2:p.Pro1106Ala
|
|
NM_017519.2:c.4750C>G
|
NP_059989.2:p.Pro1584Ala
|
|
NM_020732.3:c.4789C>G
|
NP_065783.3:p.Pro1597Ala
|
|
XM_005267069.3:c.4909C>G
|
XP_005267126.2:p.Pro1637Ala
|
|
XM_011535984.1:c.3988C>G
|
XP_011534286.1:p.Pro1330Ala
|
|
XM_011535985.1:c.3808C>G
|
XP_011534287.1:p.Pro1270Ala
|
|
XM_011535986.1:c.3568C>G
|
XP_011534288.1:p.Pro1190Ala
|
|
XM_011535987.1:c.3187C>G
|
XP_011534289.1:p.Pro1063Ala
|
|
XM_011535988.1:c.2050C>G
|
XP_011534290.1:p.Pro684Ala
|
|
NM_001346813.1:c.4909C>G
|
NP_001333742.1:p.Pro1637Ala
|
|
NM_001363725.1:c.2659C>G
|
NP_001350654.1:p.Pro887Ala
|
|
XM_011535984.2:c.5119C>G
|
XP_011534286.2:p.Pro1707Ala
|
|
XM_011535988.3:c.2050C>G
|
XP_011534290.1:p.Pro684Ala
|
|
XM_017011103.2:c.5020C>G
|
XP_016866592.1:p.Pro1674Ala
|
|
XM_017011104.1:c.4990C>G
|
XP_016866593.1:p.Pro1664Ala
|
|
XM_017011105.2:c.4960C>G
|
XP_016866594.1:p.Pro1654Ala
|
|
XM_017011106.2:c.4831C>G
|
XP_016866595.1:p.Pro1611Ala
|
|
XM_017011107.2:c.4810C>G
|
XP_016866596.1:p.Pro1604Ala
|
|
XR_002956289.1:n.5105C>G
|
|
|
NM_001363725.2:c.2659C>G
|
NP_001350654.1:p.Pro887Ala
|
|
NM_001371656.1:c.5038C>G
|
NP_001358585.1:p.Pro1680Ala
|
|
NM_001374820.1:c.5038C>G
|
NP_001361749.1:p.Pro1680Ala
|
|
NM_001374828.1:c.5158C>G
MANE Select
|
NP_001361757.1:p.Pro1720Ala
|
|
NM_017519.3:c.4999C>G
|
NP_059989.3:p.Pro1667Ala
|
|