ENST00000350026.11:c.4630C>G
|
ENSP00000055163.8:p.Pro1544Ala
|
|
ENST00000414678.8:c.4699C>G
|
ENSP00000412835.3:p.Pro1567Ala
|
|
ENST00000637015.2:c.4918C>G
|
ENSP00000489729.2:p.Pro1640Ala
|
|
ENST00000346085.10:c.4669C>G
|
ENSP00000344546.5:p.Pro1557Ala
|
|
ENST00000350026.10:c.4381C>G
|
ENSP00000055163.7:p.Pro1461Ala
|
|
ENST00000414678.7:c.2947C>G
|
ENSP00000412835.2:p.Pro983Ala
|
|
ENST00000635849.1:c.2110C>G
|
ENSP00000490948.1:p.Pro704Ala
|
|
ENST00000635957.1:c.1741C>G
|
ENSP00000490385.1:p.Pro581Ala
|
|
ENST00000636227.1:n.3252C>G
|
|
|
ENST00000636254.1:n.709C>G
|
|
|
ENST00000636930.2:c.4789C>G
MANE Select
|
ENSP00000490491.2:p.Pro1597Ala
|
|
ENST00000636940.1:n.2786C>G
|
|
|
ENST00000637015.1:c.2157C>G
|
|
|
ENST00000637568.1:c.2071C>G
|
|
|
ENST00000637741.1:n.1455C>G
|
|
|
ENST00000637810.1:c.2131C>G
|
ENSP00000489636.1:p.Pro711Ala
|
|
ENST00000637904.1:c.2290C>G
|
ENSP00000490550.1:p.Pro764Ala
|
|
ENST00000647938.1:c.4420C>G
|
ENSP00000498155.1:p.Pro1474Ala
|
|
ENST00000346085.9:c.4420C>G
|
ENSP00000344546.4:p.Pro1474Ala
|
|
ENST00000350026.9:c.4381C>G
|
ENSP00000055163.7:p.Pro1461Ala
|
|
ENST00000414678.6:c.2947C>G
|
ENSP00000412835.2:p.Pro983Ala
|
|
NM_017519.2:c.4381C>G
|
NP_059989.2:p.Pro1461Ala
|
|
NM_020732.3:c.4420C>G
|
NP_065783.3:p.Pro1474Ala
|
|
XM_005267069.3:c.4540C>G
|
XP_005267126.2:p.Pro1514Ala
|
|
XM_011535984.1:c.3619C>G
|
XP_011534286.1:p.Pro1207Ala
|
|
XM_011535985.1:c.3439C>G
|
XP_011534287.1:p.Pro1147Ala
|
|
XM_011535986.1:c.3199C>G
|
XP_011534288.1:p.Pro1067Ala
|
|
XM_011535987.1:c.2818C>G
|
XP_011534289.1:p.Pro940Ala
|
|
XM_011535988.1:c.1681C>G
|
XP_011534290.1:p.Pro561Ala
|
|
NM_001346813.1:c.4540C>G
|
NP_001333742.1:p.Pro1514Ala
|
|
NM_001363725.1:c.2290C>G
|
NP_001350654.1:p.Pro764Ala
|
|
XM_011535984.2:c.4750C>G
|
XP_011534286.2:p.Pro1584Ala
|
|
XM_011535988.3:c.1681C>G
|
XP_011534290.1:p.Pro561Ala
|
|
XM_017011103.2:c.4651C>G
|
XP_016866592.1:p.Pro1551Ala
|
|
XM_017011104.1:c.4621C>G
|
XP_016866593.1:p.Pro1541Ala
|
|
XM_017011105.2:c.4591C>G
|
XP_016866594.1:p.Pro1531Ala
|
|
XM_017011106.2:c.4462C>G
|
XP_016866595.1:p.Pro1488Ala
|
|
XM_017011107.2:c.4441C>G
|
XP_016866596.1:p.Pro1481Ala
|
|
XR_002956289.1:n.4736C>G
|
|
|
NM_001363725.2:c.2290C>G
|
NP_001350654.1:p.Pro764Ala
|
|
NM_001371656.1:c.4669C>G
|
NP_001358585.1:p.Pro1557Ala
|
|
NM_001374820.1:c.4669C>G
|
NP_001361749.1:p.Pro1557Ala
|
|
NM_001374828.1:c.4789C>G
MANE Select
|
NP_001361757.1:p.Pro1597Ala
|
|
NM_017519.3:c.4630C>G
|
NP_059989.3:p.Pro1544Ala
|
|