ENST00000350026.11:c.5011C>A
|
ENSP00000055163.8:p.Pro1671Thr
|
|
ENST00000414678.8:c.5080C>A
|
ENSP00000412835.3:p.Pro1694Thr
|
|
ENST00000637015.2:c.5299C>A
|
ENSP00000489729.2:p.Pro1767Thr
|
|
ENST00000346085.10:c.5050C>A
|
ENSP00000344546.5:p.Pro1684Thr
|
|
ENST00000350026.10:c.4762C>A
|
ENSP00000055163.7:p.Pro1588Thr
|
|
ENST00000414678.7:c.3328C>A
|
ENSP00000412835.2:p.Pro1110Thr
|
|
ENST00000635849.1:c.2491C>A
|
ENSP00000490948.1:p.Pro831Thr
|
|
ENST00000635957.1:c.2122C>A
|
ENSP00000490385.1:p.Pro708Thr
|
|
ENST00000636227.1:n.3633C>A
|
|
|
ENST00000636254.1:n.1090C>A
|
|
|
ENST00000636930.2:c.5170C>A
MANE Select
|
ENSP00000490491.2:p.Pro1724Thr
|
|
ENST00000636940.1:n.3167C>A
|
|
|
ENST00000637015.1:c.2538C>A
|
|
|
ENST00000637568.1:c.2452C>A
|
|
|
ENST00000637741.1:n.1836C>A
|
|
|
ENST00000637810.1:c.2512C>A
|
ENSP00000489636.1:p.Pro838Thr
|
|
ENST00000637904.1:c.2671C>A
|
ENSP00000490550.1:p.Pro891Thr
|
|
ENST00000647938.1:c.4801C>A
|
ENSP00000498155.1:p.Pro1601Thr
|
|
ENST00000346085.9:c.4801C>A
|
ENSP00000344546.4:p.Pro1601Thr
|
|
ENST00000350026.9:c.4762C>A
|
ENSP00000055163.7:p.Pro1588Thr
|
|
ENST00000414678.6:c.3328C>A
|
ENSP00000412835.2:p.Pro1110Thr
|
|
NM_017519.2:c.4762C>A
|
NP_059989.2:p.Pro1588Thr
|
|
NM_020732.3:c.4801C>A
|
NP_065783.3:p.Pro1601Thr
|
|
XM_005267069.3:c.4921C>A
|
XP_005267126.2:p.Pro1641Thr
|
|
XM_011535984.1:c.4000C>A
|
XP_011534286.1:p.Pro1334Thr
|
|
XM_011535985.1:c.3820C>A
|
XP_011534287.1:p.Pro1274Thr
|
|
XM_011535986.1:c.3580C>A
|
XP_011534288.1:p.Pro1194Thr
|
|
XM_011535987.1:c.3199C>A
|
XP_011534289.1:p.Pro1067Thr
|
|
XM_011535988.1:c.2062C>A
|
XP_011534290.1:p.Pro688Thr
|
|
NM_001346813.1:c.4921C>A
|
NP_001333742.1:p.Pro1641Thr
|
|
NM_001363725.1:c.2671C>A
|
NP_001350654.1:p.Pro891Thr
|
|
XM_011535984.2:c.5131C>A
|
XP_011534286.2:p.Pro1711Thr
|
|
XM_011535988.3:c.2062C>A
|
XP_011534290.1:p.Pro688Thr
|
|
XM_017011103.2:c.5032C>A
|
XP_016866592.1:p.Pro1678Thr
|
|
XM_017011104.1:c.5002C>A
|
XP_016866593.1:p.Pro1668Thr
|
|
XM_017011105.2:c.4972C>A
|
XP_016866594.1:p.Pro1658Thr
|
|
XM_017011106.2:c.4843C>A
|
XP_016866595.1:p.Pro1615Thr
|
|
XM_017011107.2:c.4822C>A
|
XP_016866596.1:p.Pro1608Thr
|
|
XR_002956289.1:n.5117C>A
|
|
|
NM_001363725.2:c.2671C>A
|
NP_001350654.1:p.Pro891Thr
|
|
NM_001371656.1:c.5050C>A
|
NP_001358585.1:p.Pro1684Thr
|
|
NM_001374820.1:c.5050C>A
|
NP_001361749.1:p.Pro1684Thr
|
|
NM_001374828.1:c.5170C>A
MANE Select
|
NP_001361757.1:p.Pro1724Thr
|
|
NM_017519.3:c.5011C>A
|
NP_059989.3:p.Pro1671Thr
|
|