ENST00000350026.11:c.2997A>T
|
ENSP00000055163.8:p.Pro999=
|
|
ENST00000414678.8:c.2907A>T
|
ENSP00000412835.3:p.Pro969=
|
|
ENST00000637015.2:c.2997A>T
|
ENSP00000489729.2:p.Pro999=
|
|
ENST00000319584.11:c.1011A>T
|
ENSP00000313006.7:p.Pro337=
|
|
ENST00000346085.10:c.3036A>T
|
ENSP00000344546.5:p.Pro1012=
|
|
ENST00000350026.10:c.2748A>T
|
ENSP00000055163.7:p.Pro916=
|
|
ENST00000414678.7:c.1155A>T
|
ENSP00000412835.2:p.Pro385=
|
|
ENST00000452544.2:n.898A>T
|
|
|
ENST00000635849.1:c.318A>T
|
ENSP00000490948.1:p.Pro106=
|
|
ENST00000636426.1:n.131A>T
|
|
|
ENST00000636930.2:c.2997A>T
MANE Select
|
ENSP00000490491.2:p.Pro999=
|
|
ENST00000637015.1:c.236A>T
|
|
|
ENST00000637568.1:c.40A>T
|
|
|
ENST00000637810.1:c.498A>T
|
ENSP00000489636.1:p.Pro166=
|
|
ENST00000637904.1:c.498A>T
|
ENSP00000490550.1:p.Pro166=
|
|
ENST00000647938.1:c.2787A>T
|
ENSP00000498155.1:p.Pro929=
|
|
ENST00000674190.1:n.1746A>T
|
|
|
ENST00000319584.10:c.1014A>T
|
ENSP00000313006.6:p.Pro338=
|
|
ENST00000346085.9:c.2787A>T
|
ENSP00000344546.4:p.Pro929=
|
|
ENST00000350026.9:c.2748A>T
|
ENSP00000055163.7:p.Pro916=
|
|
ENST00000414678.6:c.1155A>T
|
ENSP00000412835.2:p.Pro385=
|
|
ENST00000452544.1:n.844A>T
|
|
|
ENST00000478761.3:c.70A>T
|
|
|
NM_017519.2:c.2748A>T
|
NP_059989.2:p.Pro916=
|
|
NM_020732.3:c.2787A>T
|
NP_065783.3:p.Pro929=
|
|
XM_005267069.3:c.2748A>T
|
XP_005267126.2:p.Pro916=
|
|
XM_011535984.1:c.1698A>T
|
XP_011534286.1:p.Pro566=
|
|
XM_011535985.1:c.1518A>T
|
XP_011534287.1:p.Pro506=
|
|
XM_011535986.1:c.1278A>T
|
XP_011534288.1:p.Pro426=
|
|
XM_011535987.1:c.897A>T
|
XP_011534289.1:p.Pro299=
|
|
XM_011535988.1:c.-20+15652A>T
|
XP_011534290.1:n.-20+15652A>T
|
|
NM_001346813.1:c.2748A>T
|
NP_001333742.1:p.Pro916=
|
|
NM_001363725.1:c.498A>T
|
NP_001350654.1:p.Pro166=
|
|
XM_011535984.2:c.2829A>T
|
XP_011534286.2:p.Pro943=
|
|
XM_011535988.3:c.-20+15652A>T
|
XP_011534290.1:n.-20+15652A>T
|
|
XM_017011103.2:c.2829A>T
|
XP_016866592.1:p.Pro943=
|
|
XM_017011104.1:c.2829A>T
|
XP_016866593.1:p.Pro943=
|
|
XM_017011105.2:c.2829A>T
|
XP_016866594.1:p.Pro943=
|
|
XM_017011106.2:c.2829A>T
|
XP_016866595.1:p.Pro943=
|
|
XM_017011107.2:c.2649A>T
|
XP_016866596.1:p.Pro883=
|
|
XR_002956289.1:n.2912A>T
|
|
|
NM_001363725.2:c.498A>T
|
NP_001350654.1:p.Pro166=
|
|
NM_001371656.1:c.3036A>T
|
NP_001358585.1:p.Pro1012=
|
|
NM_001374820.1:c.3036A>T
|
NP_001361749.1:p.Pro1012=
|
|
NM_001374828.1:c.2997A>T
MANE Select
|
NP_001361757.1:p.Pro999=
|
|
NM_017519.3:c.2997A>T
|
NP_059989.3:p.Pro999=
|
|