ENST00000350026.11:c.3875A>C
|
ENSP00000055163.8:p.Gln1292Pro
|
|
ENST00000414678.8:c.3944A>C
|
ENSP00000412835.3:p.Gln1315Pro
|
|
ENST00000637015.2:c.4163A>C
|
ENSP00000489729.2:p.Gln1388Pro
|
|
ENST00000346085.10:c.3914A>C
|
ENSP00000344546.5:p.Gln1305Pro
|
|
ENST00000350026.10:c.3626A>C
|
ENSP00000055163.7:p.Gln1209Pro
|
|
ENST00000414678.7:c.2192A>C
|
ENSP00000412835.2:p.Gln731Pro
|
|
ENST00000635849.1:c.1355A>C
|
ENSP00000490948.1:p.Gln452Pro
|
|
ENST00000635957.1:c.989A>C
|
ENSP00000490385.1:p.Gln330Pro
|
|
ENST00000636930.2:c.4034A>C
MANE Select
|
ENSP00000490491.2:p.Gln1345Pro
|
|
ENST00000636940.1:n.2031A>C
|
|
|
ENST00000637015.1:c.1402A>C
|
|
|
ENST00000637568.1:c.1316A>C
|
|
|
ENST00000637741.1:n.700A>C
|
|
|
ENST00000637810.1:c.1376A>C
|
ENSP00000489636.1:p.Gln459Pro
|
|
ENST00000637904.1:c.1535A>C
|
ENSP00000490550.1:p.Gln512Pro
|
|
ENST00000647938.1:c.3665A>C
|
ENSP00000498155.1:p.Gln1222Pro
|
|
ENST00000346085.9:c.3665A>C
|
ENSP00000344546.4:p.Gln1222Pro
|
|
ENST00000350026.9:c.3626A>C
|
ENSP00000055163.7:p.Gln1209Pro
|
|
ENST00000414678.6:c.2192A>C
|
ENSP00000412835.2:p.Gln731Pro
|
|
NM_017519.2:c.3626A>C
|
NP_059989.2:p.Gln1209Pro
|
|
NM_020732.3:c.3665A>C
|
NP_065783.3:p.Gln1222Pro
|
|
XM_005267069.3:c.3785A>C
|
XP_005267126.2:p.Gln1262Pro
|
|
XM_011535984.1:c.2864A>C
|
XP_011534286.1:p.Gln955Pro
|
|
XM_011535985.1:c.2684A>C
|
XP_011534287.1:p.Gln895Pro
|
|
XM_011535986.1:c.2444A>C
|
XP_011534288.1:p.Gln815Pro
|
|
XM_011535987.1:c.2063A>C
|
XP_011534289.1:p.Gln688Pro
|
|
XM_011535988.1:c.926A>C
|
XP_011534290.1:p.Gln309Pro
|
|
NM_001346813.1:c.3785A>C
|
NP_001333742.1:p.Gln1262Pro
|
|
NM_001363725.1:c.1535A>C
|
NP_001350654.1:p.Gln512Pro
|
|
XM_011535984.2:c.3995A>C
|
XP_011534286.2:p.Gln1332Pro
|
|
XM_011535988.3:c.926A>C
|
XP_011534290.1:p.Gln309Pro
|
|
XM_017011103.2:c.3896A>C
|
XP_016866592.1:p.Gln1299Pro
|
|
XM_017011104.1:c.3866A>C
|
XP_016866593.1:p.Gln1289Pro
|
|
XM_017011105.2:c.3836A>C
|
XP_016866594.1:p.Gln1279Pro
|
|
XM_017011106.2:c.3707A>C
|
XP_016866595.1:p.Gln1236Pro
|
|
XM_017011107.2:c.3686A>C
|
XP_016866596.1:p.Gln1229Pro
|
|
XR_002956289.1:n.4078A>C
|
|
|
NM_001363725.2:c.1535A>C
|
NP_001350654.1:p.Gln512Pro
|
|
NM_001371656.1:c.3914A>C
|
NP_001358585.1:p.Gln1305Pro
|
|
NM_001374820.1:c.3914A>C
|
NP_001361749.1:p.Gln1305Pro
|
|
NM_001374828.1:c.4034A>C
MANE Select
|
NP_001361757.1:p.Gln1345Pro
|
|
NM_017519.3:c.3875A>C
|
NP_059989.3:p.Gln1292Pro
|
|