ENST00000350026.11:c.3052G>T
|
ENSP00000055163.8:p.Ala1018Ser
|
|
ENST00000414678.8:c.2962G>T
|
ENSP00000412835.3:p.Ala988Ser
|
|
ENST00000637015.2:c.3052G>T
|
ENSP00000489729.2:p.Ala1018Ser
|
|
ENST00000319584.11:c.1066G>T
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ENSP00000313006.7:p.Ala356Ser
|
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ENST00000346085.10:c.3091G>T
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ENSP00000344546.5:p.Ala1031Ser
|
|
ENST00000350026.10:c.2803G>T
|
ENSP00000055163.7:p.Ala935Ser
|
|
ENST00000414678.7:c.1210G>T
|
ENSP00000412835.2:p.Ala404Ser
|
|
ENST00000452544.2:n.953G>T
|
|
|
ENST00000635849.1:c.373G>T
|
ENSP00000490948.1:p.Ala125Ser
|
|
ENST00000635957.1:c.7G>T
|
ENSP00000490385.1:p.Ala3Ser
|
|
ENST00000636426.1:n.186G>T
|
|
|
ENST00000636930.2:c.3052G>T
MANE Select
|
ENSP00000490491.2:p.Ala1018Ser
|
|
ENST00000637015.1:c.291G>T
|
|
|
ENST00000637568.1:c.95G>T
|
|
|
ENST00000637810.1:c.553G>T
|
ENSP00000489636.1:p.Ala185Ser
|
|
ENST00000637904.1:c.553G>T
|
ENSP00000490550.1:p.Ala185Ser
|
|
ENST00000647938.1:c.2842G>T
|
ENSP00000498155.1:p.Ala948Ser
|
|
ENST00000674190.1:n.1801G>T
|
|
|
ENST00000319584.10:c.1069G>T
|
ENSP00000313006.6:p.Ala357Ser
|
|
ENST00000346085.9:c.2842G>T
|
ENSP00000344546.4:p.Ala948Ser
|
|
ENST00000350026.9:c.2803G>T
|
ENSP00000055163.7:p.Ala935Ser
|
|
ENST00000400790.3:c.4G>T
|
ENSP00000383596.3:p.Ala2Ser
|
|
ENST00000414678.6:c.1210G>T
|
ENSP00000412835.2:p.Ala404Ser
|
|
ENST00000452544.1:n.899G>T
|
|
|
ENST00000478761.3:c.125G>T
|
|
|
NM_017519.2:c.2803G>T
|
NP_059989.2:p.Ala935Ser
|
|
NM_020732.3:c.2842G>T
|
NP_065783.3:p.Ala948Ser
|
|
XM_005267069.3:c.2803G>T
|
XP_005267126.2:p.Ala935Ser
|
|
XM_011535984.1:c.1753G>T
|
XP_011534286.1:p.Ala585Ser
|
|
XM_011535985.1:c.1573G>T
|
XP_011534287.1:p.Ala525Ser
|
|
XM_011535986.1:c.1333G>T
|
XP_011534288.1:p.Ala445Ser
|
|
XM_011535987.1:c.952G>T
|
XP_011534289.1:p.Ala318Ser
|
|
XM_011535988.1:c.-20+15707G>T
|
XP_011534290.1:n.-20+15707G>T
|
|
NM_001346813.1:c.2803G>T
|
NP_001333742.1:p.Ala935Ser
|
|
NM_001363725.1:c.553G>T
|
NP_001350654.1:p.Ala185Ser
|
|
XM_011535984.2:c.2884G>T
|
XP_011534286.2:p.Ala962Ser
|
|
XM_011535988.3:c.-20+15707G>T
|
XP_011534290.1:n.-20+15707G>T
|
|
XM_017011103.2:c.2884G>T
|
XP_016866592.1:p.Ala962Ser
|
|
XM_017011104.1:c.2884G>T
|
XP_016866593.1:p.Ala962Ser
|
|
XM_017011105.2:c.2884G>T
|
XP_016866594.1:p.Ala962Ser
|
|
XM_017011106.2:c.2884G>T
|
XP_016866595.1:p.Ala962Ser
|
|
XM_017011107.2:c.2704G>T
|
XP_016866596.1:p.Ala902Ser
|
|
XR_002956289.1:n.2967G>T
|
|
|
NM_001363725.2:c.553G>T
|
NP_001350654.1:p.Ala185Ser
|
|
NM_001371656.1:c.3091G>T
|
NP_001358585.1:p.Ala1031Ser
|
|
NM_001374820.1:c.3091G>T
|
NP_001361749.1:p.Ala1031Ser
|
|
NM_001374828.1:c.3052G>T
MANE Select
|
NP_001361757.1:p.Ala1018Ser
|
|
NM_017519.3:c.3052G>T
|
NP_059989.3:p.Ala1018Ser
|
|