ENST00000350026.11:c.3052G>C
|
ENSP00000055163.8:p.Ala1018Pro
|
|
ENST00000414678.8:c.2962G>C
|
ENSP00000412835.3:p.Ala988Pro
|
|
ENST00000637015.2:c.3052G>C
|
ENSP00000489729.2:p.Ala1018Pro
|
|
ENST00000319584.11:c.1066G>C
|
ENSP00000313006.7:p.Ala356Pro
|
|
ENST00000346085.10:c.3091G>C
|
ENSP00000344546.5:p.Ala1031Pro
|
|
ENST00000350026.10:c.2803G>C
|
ENSP00000055163.7:p.Ala935Pro
|
|
ENST00000414678.7:c.1210G>C
|
ENSP00000412835.2:p.Ala404Pro
|
|
ENST00000452544.2:n.953G>C
|
|
|
ENST00000635849.1:c.373G>C
|
ENSP00000490948.1:p.Ala125Pro
|
|
ENST00000635957.1:c.7G>C
|
ENSP00000490385.1:p.Ala3Pro
|
|
ENST00000636426.1:n.186G>C
|
|
|
ENST00000636930.2:c.3052G>C
MANE Select
|
ENSP00000490491.2:p.Ala1018Pro
|
|
ENST00000637015.1:c.291G>C
|
|
|
ENST00000637568.1:c.95G>C
|
|
|
ENST00000637810.1:c.553G>C
|
ENSP00000489636.1:p.Ala185Pro
|
|
ENST00000637904.1:c.553G>C
|
ENSP00000490550.1:p.Ala185Pro
|
|
ENST00000647938.1:c.2842G>C
|
ENSP00000498155.1:p.Ala948Pro
|
|
ENST00000674190.1:n.1801G>C
|
|
|
ENST00000319584.10:c.1069G>C
|
ENSP00000313006.6:p.Ala357Pro
|
|
ENST00000346085.9:c.2842G>C
|
ENSP00000344546.4:p.Ala948Pro
|
|
ENST00000350026.9:c.2803G>C
|
ENSP00000055163.7:p.Ala935Pro
|
|
ENST00000400790.3:c.4G>C
|
ENSP00000383596.3:p.Ala2Pro
|
|
ENST00000414678.6:c.1210G>C
|
ENSP00000412835.2:p.Ala404Pro
|
|
ENST00000452544.1:n.899G>C
|
|
|
ENST00000478761.3:c.125G>C
|
|
|
NM_017519.2:c.2803G>C
|
NP_059989.2:p.Ala935Pro
|
|
NM_020732.3:c.2842G>C
|
NP_065783.3:p.Ala948Pro
|
|
XM_005267069.3:c.2803G>C
|
XP_005267126.2:p.Ala935Pro
|
|
XM_011535984.1:c.1753G>C
|
XP_011534286.1:p.Ala585Pro
|
|
XM_011535985.1:c.1573G>C
|
XP_011534287.1:p.Ala525Pro
|
|
XM_011535986.1:c.1333G>C
|
XP_011534288.1:p.Ala445Pro
|
|
XM_011535987.1:c.952G>C
|
XP_011534289.1:p.Ala318Pro
|
|
XM_011535988.1:c.-20+15707G>C
|
XP_011534290.1:n.-20+15707G>C
|
|
NM_001346813.1:c.2803G>C
|
NP_001333742.1:p.Ala935Pro
|
|
NM_001363725.1:c.553G>C
|
NP_001350654.1:p.Ala185Pro
|
|
XM_011535984.2:c.2884G>C
|
XP_011534286.2:p.Ala962Pro
|
|
XM_011535988.3:c.-20+15707G>C
|
XP_011534290.1:n.-20+15707G>C
|
|
XM_017011103.2:c.2884G>C
|
XP_016866592.1:p.Ala962Pro
|
|
XM_017011104.1:c.2884G>C
|
XP_016866593.1:p.Ala962Pro
|
|
XM_017011105.2:c.2884G>C
|
XP_016866594.1:p.Ala962Pro
|
|
XM_017011106.2:c.2884G>C
|
XP_016866595.1:p.Ala962Pro
|
|
XM_017011107.2:c.2704G>C
|
XP_016866596.1:p.Ala902Pro
|
|
XR_002956289.1:n.2967G>C
|
|
|
NM_001363725.2:c.553G>C
|
NP_001350654.1:p.Ala185Pro
|
|
NM_001371656.1:c.3091G>C
|
NP_001358585.1:p.Ala1031Pro
|
|
NM_001374820.1:c.3091G>C
|
NP_001361749.1:p.Ala1031Pro
|
|
NM_001374828.1:c.3052G>C
MANE Select
|
NP_001361757.1:p.Ala1018Pro
|
|
NM_017519.3:c.3052G>C
|
NP_059989.3:p.Ala1018Pro
|
|