ENST00000350026.11:c.3914G>T
|
ENSP00000055163.8:p.Ser1305Ile
|
|
ENST00000414678.8:c.3983G>T
|
ENSP00000412835.3:p.Ser1328Ile
|
|
ENST00000637015.2:c.4202G>T
|
ENSP00000489729.2:p.Ser1401Ile
|
|
ENST00000346085.10:c.3953G>T
|
ENSP00000344546.5:p.Ser1318Ile
|
|
ENST00000350026.10:c.3665G>T
|
ENSP00000055163.7:p.Ser1222Ile
|
|
ENST00000414678.7:c.2231G>T
|
ENSP00000412835.2:p.Ser744Ile
|
|
ENST00000635849.1:c.1394G>T
|
ENSP00000490948.1:p.Ser465Ile
|
|
ENST00000635957.1:c.1025G>T
|
ENSP00000490385.1:p.Ser342Ile
|
|
ENST00000636930.2:c.4073G>T
MANE Select
|
ENSP00000490491.2:p.Ser1358Ile
|
|
ENST00000636940.1:n.2070G>T
|
|
|
ENST00000637015.1:c.1441G>T
|
|
|
ENST00000637568.1:c.1355G>T
|
|
|
ENST00000637741.1:n.739G>T
|
|
|
ENST00000637810.1:c.1415G>T
|
ENSP00000489636.1:p.Ser472Ile
|
|
ENST00000637904.1:c.1574G>T
|
ENSP00000490550.1:p.Ser525Ile
|
|
ENST00000647938.1:c.3704G>T
|
ENSP00000498155.1:p.Ser1235Ile
|
|
ENST00000346085.9:c.3704G>T
|
ENSP00000344546.4:p.Ser1235Ile
|
|
ENST00000350026.9:c.3665G>T
|
ENSP00000055163.7:p.Ser1222Ile
|
|
ENST00000414678.6:c.2231G>T
|
ENSP00000412835.2:p.Ser744Ile
|
|
NM_017519.2:c.3665G>T
|
NP_059989.2:p.Ser1222Ile
|
|
NM_020732.3:c.3704G>T
|
NP_065783.3:p.Ser1235Ile
|
|
XM_005267069.3:c.3824G>T
|
XP_005267126.2:p.Ser1275Ile
|
|
XM_011535984.1:c.2903G>T
|
XP_011534286.1:p.Ser968Ile
|
|
XM_011535985.1:c.2723G>T
|
XP_011534287.1:p.Ser908Ile
|
|
XM_011535986.1:c.2483G>T
|
XP_011534288.1:p.Ser828Ile
|
|
XM_011535987.1:c.2102G>T
|
XP_011534289.1:p.Ser701Ile
|
|
XM_011535988.1:c.965G>T
|
XP_011534290.1:p.Ser322Ile
|
|
NM_001346813.1:c.3824G>T
|
NP_001333742.1:p.Ser1275Ile
|
|
NM_001363725.1:c.1574G>T
|
NP_001350654.1:p.Ser525Ile
|
|
XM_011535984.2:c.4034G>T
|
XP_011534286.2:p.Ser1345Ile
|
|
XM_011535988.3:c.965G>T
|
XP_011534290.1:p.Ser322Ile
|
|
XM_017011103.2:c.3935G>T
|
XP_016866592.1:p.Ser1312Ile
|
|
XM_017011104.1:c.3905G>T
|
XP_016866593.1:p.Ser1302Ile
|
|
XM_017011105.2:c.3875G>T
|
XP_016866594.1:p.Ser1292Ile
|
|
XM_017011106.2:c.3746G>T
|
XP_016866595.1:p.Ser1249Ile
|
|
XM_017011107.2:c.3725G>T
|
XP_016866596.1:p.Ser1242Ile
|
|
XR_002956289.1:n.4117G>T
|
|
|
NM_001363725.2:c.1574G>T
|
NP_001350654.1:p.Ser525Ile
|
|
NM_001371656.1:c.3953G>T
|
NP_001358585.1:p.Ser1318Ile
|
|
NM_001374820.1:c.3953G>T
|
NP_001361749.1:p.Ser1318Ile
|
|
NM_001374828.1:c.4073G>T
MANE Select
|
NP_001361757.1:p.Ser1358Ile
|
|
NM_017519.3:c.3914G>T
|
NP_059989.3:p.Ser1305Ile
|
|