ENST00000350026.11:c.4973C>G
|
ENSP00000055163.8:p.Pro1658Arg
|
|
ENST00000414678.8:c.5042C>G
|
ENSP00000412835.3:p.Pro1681Arg
|
|
ENST00000637015.2:c.5261C>G
|
ENSP00000489729.2:p.Pro1754Arg
|
|
ENST00000346085.10:c.5012C>G
|
ENSP00000344546.5:p.Pro1671Arg
|
|
ENST00000350026.10:c.4724C>G
|
ENSP00000055163.7:p.Pro1575Arg
|
|
ENST00000414678.7:c.3290C>G
|
ENSP00000412835.2:p.Pro1097Arg
|
|
ENST00000635849.1:c.2453C>G
|
ENSP00000490948.1:p.Pro818Arg
|
|
ENST00000635957.1:c.2084C>G
|
ENSP00000490385.1:p.Pro695Arg
|
|
ENST00000636227.1:n.3595C>G
|
|
|
ENST00000636254.1:n.1052C>G
|
|
|
ENST00000636930.2:c.5132C>G
MANE Select
|
ENSP00000490491.2:p.Pro1711Arg
|
|
ENST00000636940.1:n.3129C>G
|
|
|
ENST00000637015.1:c.2500C>G
|
|
|
ENST00000637568.1:c.2414C>G
|
|
|
ENST00000637741.1:n.1798C>G
|
|
|
ENST00000637810.1:c.2474C>G
|
ENSP00000489636.1:p.Pro825Arg
|
|
ENST00000637904.1:c.2633C>G
|
ENSP00000490550.1:p.Pro878Arg
|
|
ENST00000647938.1:c.4763C>G
|
ENSP00000498155.1:p.Pro1588Arg
|
|
ENST00000346085.9:c.4763C>G
|
ENSP00000344546.4:p.Pro1588Arg
|
|
ENST00000350026.9:c.4724C>G
|
ENSP00000055163.7:p.Pro1575Arg
|
|
ENST00000414678.6:c.3290C>G
|
ENSP00000412835.2:p.Pro1097Arg
|
|
NM_017519.2:c.4724C>G
|
NP_059989.2:p.Pro1575Arg
|
|
NM_020732.3:c.4763C>G
|
NP_065783.3:p.Pro1588Arg
|
|
XM_005267069.3:c.4883C>G
|
XP_005267126.2:p.Pro1628Arg
|
|
XM_011535984.1:c.3962C>G
|
XP_011534286.1:p.Pro1321Arg
|
|
XM_011535985.1:c.3782C>G
|
XP_011534287.1:p.Pro1261Arg
|
|
XM_011535986.1:c.3542C>G
|
XP_011534288.1:p.Pro1181Arg
|
|
XM_011535987.1:c.3161C>G
|
XP_011534289.1:p.Pro1054Arg
|
|
XM_011535988.1:c.2024C>G
|
XP_011534290.1:p.Pro675Arg
|
|
NM_001346813.1:c.4883C>G
|
NP_001333742.1:p.Pro1628Arg
|
|
NM_001363725.1:c.2633C>G
|
NP_001350654.1:p.Pro878Arg
|
|
XM_011535984.2:c.5093C>G
|
XP_011534286.2:p.Pro1698Arg
|
|
XM_011535988.3:c.2024C>G
|
XP_011534290.1:p.Pro675Arg
|
|
XM_017011103.2:c.4994C>G
|
XP_016866592.1:p.Pro1665Arg
|
|
XM_017011104.1:c.4964C>G
|
XP_016866593.1:p.Pro1655Arg
|
|
XM_017011105.2:c.4934C>G
|
XP_016866594.1:p.Pro1645Arg
|
|
XM_017011106.2:c.4805C>G
|
XP_016866595.1:p.Pro1602Arg
|
|
XM_017011107.2:c.4784C>G
|
XP_016866596.1:p.Pro1595Arg
|
|
XR_002956289.1:n.5079C>G
|
|
|
NM_001363725.2:c.2633C>G
|
NP_001350654.1:p.Pro878Arg
|
|
NM_001371656.1:c.5012C>G
|
NP_001358585.1:p.Pro1671Arg
|
|
NM_001374820.1:c.5012C>G
|
NP_001361749.1:p.Pro1671Arg
|
|
NM_001374828.1:c.5132C>G
MANE Select
|
NP_001361757.1:p.Pro1711Arg
|
|
NM_017519.3:c.4973C>G
|
NP_059989.3:p.Pro1658Arg
|
|