ENST00000350026.11:c.2910A>G
|
ENSP00000055163.8:p.Pro970=
|
|
ENST00000414678.8:c.2820A>G
|
ENSP00000412835.3:p.Pro940=
|
|
ENST00000637015.2:c.2910A>G
|
ENSP00000489729.2:p.Pro970=
|
|
ENST00000319584.11:c.924A>G
|
ENSP00000313006.7:p.Pro308=
|
|
ENST00000346085.10:c.2949A>G
|
ENSP00000344546.5:p.Pro983=
|
|
ENST00000350026.10:c.2661A>G
|
ENSP00000055163.7:p.Pro887=
|
|
ENST00000414678.7:c.1068A>G
|
ENSP00000412835.2:p.Pro356=
|
|
ENST00000452544.2:n.811A>G
|
|
|
ENST00000635849.1:c.231A>G
|
ENSP00000490948.1:p.Pro77=
|
|
ENST00000636426.1:n.44A>G
|
|
|
ENST00000636930.2:c.2910A>G
MANE Select
|
ENSP00000490491.2:p.Pro970=
|
|
ENST00000637015.1:c.149A>G
|
|
|
ENST00000637810.1:c.411A>G
|
ENSP00000489636.1:p.Pro137=
|
|
ENST00000637904.1:c.411A>G
|
ENSP00000490550.1:p.Pro137=
|
|
ENST00000647938.1:c.2700A>G
|
ENSP00000498155.1:p.Pro900=
|
|
ENST00000674190.1:n.1659A>G
|
|
|
ENST00000319584.10:c.927A>G
|
ENSP00000313006.6:p.Pro309=
|
|
ENST00000346085.9:c.2700A>G
|
ENSP00000344546.4:p.Pro900=
|
|
ENST00000350026.9:c.2661A>G
|
ENSP00000055163.7:p.Pro887=
|
|
ENST00000414678.6:c.1068A>G
|
ENSP00000412835.2:p.Pro356=
|
|
ENST00000452544.1:n.757A>G
|
|
|
NM_017519.2:c.2661A>G
|
NP_059989.2:p.Pro887=
|
|
NM_020732.3:c.2700A>G
|
NP_065783.3:p.Pro900=
|
|
XM_005267069.3:c.2661A>G
|
XP_005267126.2:p.Pro887=
|
|
XM_011535984.1:c.1611A>G
|
XP_011534286.1:p.Pro537=
|
|
XM_011535985.1:c.1431A>G
|
XP_011534287.1:p.Pro477=
|
|
XM_011535986.1:c.1191A>G
|
XP_011534288.1:p.Pro397=
|
|
XM_011535987.1:c.810A>G
|
XP_011534289.1:p.Pro270=
|
|
XM_011535988.1:c.-20+15565A>G
|
XP_011534290.1:n.-20+15565A>G
|
|
NM_001346813.1:c.2661A>G
|
NP_001333742.1:p.Pro887=
|
|
NM_001363725.1:c.411A>G
|
NP_001350654.1:p.Pro137=
|
|
XM_011535984.2:c.2742A>G
|
XP_011534286.2:p.Pro914=
|
|
XM_011535988.3:c.-20+15565A>G
|
XP_011534290.1:n.-20+15565A>G
|
|
XM_017011103.2:c.2742A>G
|
XP_016866592.1:p.Pro914=
|
|
XM_017011104.1:c.2742A>G
|
XP_016866593.1:p.Pro914=
|
|
XM_017011105.2:c.2742A>G
|
XP_016866594.1:p.Pro914=
|
|
XM_017011106.2:c.2742A>G
|
XP_016866595.1:p.Pro914=
|
|
XM_017011107.2:c.2562A>G
|
XP_016866596.1:p.Pro854=
|
|
XR_002956289.1:n.2825A>G
|
|
|
NM_001363725.2:c.411A>G
|
NP_001350654.1:p.Pro137=
|
|
NM_001371656.1:c.2949A>G
|
NP_001358585.1:p.Pro983=
|
|
NM_001374820.1:c.2949A>G
|
NP_001361749.1:p.Pro983=
|
|
NM_001374828.1:c.2910A>G
MANE Select
|
NP_001361757.1:p.Pro970=
|
|
NM_017519.3:c.2910A>G
|
NP_059989.3:p.Pro970=
|
|