ENST00000350026.11:c.3815C>T
|
ENSP00000055163.8:p.Ser1272Phe
|
|
ENST00000414678.8:c.3884C>T
|
ENSP00000412835.3:p.Ser1295Phe
|
|
ENST00000637015.2:c.4103C>T
|
ENSP00000489729.2:p.Ser1368Phe
|
|
ENST00000346085.10:c.3854C>T
|
ENSP00000344546.5:p.Ser1285Phe
|
|
ENST00000350026.10:c.3566C>T
|
ENSP00000055163.7:p.Ser1189Phe
|
|
ENST00000414678.7:c.2132C>T
|
ENSP00000412835.2:p.Ser711Phe
|
|
ENST00000635849.1:c.1295C>T
|
ENSP00000490948.1:p.Ser432Phe
|
|
ENST00000635957.1:c.929C>T
|
ENSP00000490385.1:p.Ser310Phe
|
|
ENST00000636930.2:c.3974C>T
MANE Select
|
ENSP00000490491.2:p.Ser1325Phe
|
|
ENST00000636940.1:n.1971C>T
|
|
|
ENST00000637015.1:c.1342C>T
|
|
|
ENST00000637568.1:c.1256C>T
|
|
|
ENST00000637741.1:n.640C>T
|
|
|
ENST00000637810.1:c.1316C>T
|
ENSP00000489636.1:p.Ser439Phe
|
|
ENST00000637904.1:c.1475C>T
|
ENSP00000490550.1:p.Ser492Phe
|
|
ENST00000647938.1:c.3605C>T
|
ENSP00000498155.1:p.Ser1202Phe
|
|
ENST00000346085.9:c.3605C>T
|
ENSP00000344546.4:p.Ser1202Phe
|
|
ENST00000350026.9:c.3566C>T
|
ENSP00000055163.7:p.Ser1189Phe
|
|
ENST00000414678.6:c.2132C>T
|
ENSP00000412835.2:p.Ser711Phe
|
|
NM_017519.2:c.3566C>T
|
NP_059989.2:p.Ser1189Phe
|
|
NM_020732.3:c.3605C>T
|
NP_065783.3:p.Ser1202Phe
|
|
XM_005267069.3:c.3725C>T
|
XP_005267126.2:p.Ser1242Phe
|
|
XM_011535984.1:c.2804C>T
|
XP_011534286.1:p.Ser935Phe
|
|
XM_011535985.1:c.2624C>T
|
XP_011534287.1:p.Ser875Phe
|
|
XM_011535986.1:c.2384C>T
|
XP_011534288.1:p.Ser795Phe
|
|
XM_011535987.1:c.2003C>T
|
XP_011534289.1:p.Ser668Phe
|
|
XM_011535988.1:c.866C>T
|
XP_011534290.1:p.Ser289Phe
|
|
NM_001346813.1:c.3725C>T
|
NP_001333742.1:p.Ser1242Phe
|
|
NM_001363725.1:c.1475C>T
|
NP_001350654.1:p.Ser492Phe
|
|
XM_011535984.2:c.3935C>T
|
XP_011534286.2:p.Ser1312Phe
|
|
XM_011535988.3:c.866C>T
|
XP_011534290.1:p.Ser289Phe
|
|
XM_017011103.2:c.3836C>T
|
XP_016866592.1:p.Ser1279Phe
|
|
XM_017011104.1:c.3806C>T
|
XP_016866593.1:p.Ser1269Phe
|
|
XM_017011105.2:c.3776C>T
|
XP_016866594.1:p.Ser1259Phe
|
|
XM_017011106.2:c.3647C>T
|
XP_016866595.1:p.Ser1216Phe
|
|
XM_017011107.2:c.3626C>T
|
XP_016866596.1:p.Ser1209Phe
|
|
XR_002956289.1:n.4018C>T
|
|
|
NM_001363725.2:c.1475C>T
|
NP_001350654.1:p.Ser492Phe
|
|
NM_001371656.1:c.3854C>T
|
NP_001358585.1:p.Ser1285Phe
|
|
NM_001374820.1:c.3854C>T
|
NP_001361749.1:p.Ser1285Phe
|
|
NM_001374828.1:c.3974C>T
MANE Select
|
NP_001361757.1:p.Ser1325Phe
|
|
NM_017519.3:c.3815C>T
|
NP_059989.3:p.Ser1272Phe
|
|