ENST00000350026.11:c.5011C>G
|
ENSP00000055163.8:p.Pro1671Ala
|
|
ENST00000414678.8:c.5080C>G
|
ENSP00000412835.3:p.Pro1694Ala
|
|
ENST00000637015.2:c.5299C>G
|
ENSP00000489729.2:p.Pro1767Ala
|
|
ENST00000346085.10:c.5050C>G
|
ENSP00000344546.5:p.Pro1684Ala
|
|
ENST00000350026.10:c.4762C>G
|
ENSP00000055163.7:p.Pro1588Ala
|
|
ENST00000414678.7:c.3328C>G
|
ENSP00000412835.2:p.Pro1110Ala
|
|
ENST00000635849.1:c.2491C>G
|
ENSP00000490948.1:p.Pro831Ala
|
|
ENST00000635957.1:c.2122C>G
|
ENSP00000490385.1:p.Pro708Ala
|
|
ENST00000636227.1:n.3633C>G
|
|
|
ENST00000636254.1:n.1090C>G
|
|
|
ENST00000636930.2:c.5170C>G
MANE Select
|
ENSP00000490491.2:p.Pro1724Ala
|
|
ENST00000636940.1:n.3167C>G
|
|
|
ENST00000637015.1:c.2538C>G
|
|
|
ENST00000637568.1:c.2452C>G
|
|
|
ENST00000637741.1:n.1836C>G
|
|
|
ENST00000637810.1:c.2512C>G
|
ENSP00000489636.1:p.Pro838Ala
|
|
ENST00000637904.1:c.2671C>G
|
ENSP00000490550.1:p.Pro891Ala
|
|
ENST00000647938.1:c.4801C>G
|
ENSP00000498155.1:p.Pro1601Ala
|
|
ENST00000346085.9:c.4801C>G
|
ENSP00000344546.4:p.Pro1601Ala
|
|
ENST00000350026.9:c.4762C>G
|
ENSP00000055163.7:p.Pro1588Ala
|
|
ENST00000414678.6:c.3328C>G
|
ENSP00000412835.2:p.Pro1110Ala
|
|
NM_017519.2:c.4762C>G
|
NP_059989.2:p.Pro1588Ala
|
|
NM_020732.3:c.4801C>G
|
NP_065783.3:p.Pro1601Ala
|
|
XM_005267069.3:c.4921C>G
|
XP_005267126.2:p.Pro1641Ala
|
|
XM_011535984.1:c.4000C>G
|
XP_011534286.1:p.Pro1334Ala
|
|
XM_011535985.1:c.3820C>G
|
XP_011534287.1:p.Pro1274Ala
|
|
XM_011535986.1:c.3580C>G
|
XP_011534288.1:p.Pro1194Ala
|
|
XM_011535987.1:c.3199C>G
|
XP_011534289.1:p.Pro1067Ala
|
|
XM_011535988.1:c.2062C>G
|
XP_011534290.1:p.Pro688Ala
|
|
NM_001346813.1:c.4921C>G
|
NP_001333742.1:p.Pro1641Ala
|
|
NM_001363725.1:c.2671C>G
|
NP_001350654.1:p.Pro891Ala
|
|
XM_011535984.2:c.5131C>G
|
XP_011534286.2:p.Pro1711Ala
|
|
XM_011535988.3:c.2062C>G
|
XP_011534290.1:p.Pro688Ala
|
|
XM_017011103.2:c.5032C>G
|
XP_016866592.1:p.Pro1678Ala
|
|
XM_017011104.1:c.5002C>G
|
XP_016866593.1:p.Pro1668Ala
|
|
XM_017011105.2:c.4972C>G
|
XP_016866594.1:p.Pro1658Ala
|
|
XM_017011106.2:c.4843C>G
|
XP_016866595.1:p.Pro1615Ala
|
|
XM_017011107.2:c.4822C>G
|
XP_016866596.1:p.Pro1608Ala
|
|
XR_002956289.1:n.5117C>G
|
|
|
NM_001363725.2:c.2671C>G
|
NP_001350654.1:p.Pro891Ala
|
|
NM_001371656.1:c.5050C>G
|
NP_001358585.1:p.Pro1684Ala
|
|
NM_001374820.1:c.5050C>G
|
NP_001361749.1:p.Pro1684Ala
|
|
NM_001374828.1:c.5170C>G
MANE Select
|
NP_001361757.1:p.Pro1724Ala
|
|
NM_017519.3:c.5011C>G
|
NP_059989.3:p.Pro1671Ala
|
|