ENST00000692585.1:c.325G>T
|
ENSP00000509200.1:p.Ala109Ser
|
|
ENST00000294309.8:c.1468G>T
MANE Select
|
ENSP00000294309.3:p.Ala490Ser
|
|
ENST00000635811.1:c.1468G>T
|
ENSP00000490341.1:p.Ala490Ser
|
|
ENST00000637084.1:c.325G>T
|
ENSP00000490615.1:p.Ala109Ser
|
|
ENST00000637342.1:c.1468G>T
|
ENSP00000490171.1:p.Ala490Ser
|
|
ENST00000637504.1:c.1468G>T
|
ENSP00000489759.1:p.Ala490Ser
|
|
ENST00000294309.7:c.1468G>T
|
ENSP00000294309.3:p.Ala490Ser
|
|
ENST00000442692.2:n.1061G>T
|
|
|
ENST00000535009.5:n.1277G>T
|
|
|
ENST00000542467.1:c.1468G>T
|
ENSP00000445551.1:p.Ala490Ser
|
|
NM_139075.3:c.1468G>T
|
NP_620714.2:p.Ala490Ser
|
|
XM_005273824.2:c.1465G>T
|
XP_005273881.1:p.Ala489Ser
|
|
XM_005273826.2:c.1213G>T
|
XP_005273883.1:p.Ala405Ser
|
|
XM_005273827.2:c.1468G>T
|
XP_005273884.1:p.Ala490Ser
|
|
XM_005273828.2:c.1468G>T
|
XP_005273885.1:p.Ala490Ser
|
|
XM_005273830.2:c.775G>T
|
XP_005273887.1:p.Ala259Ser
|
|
XM_005273831.2:c.775G>T
|
XP_005273888.1:p.Ala259Ser
|
|
XM_005273832.2:c.745G>T
|
XP_005273889.1:p.Ala249Ser
|
|
XM_006718453.2:c.1468G>T
|
XP_006718516.1:p.Ala490Ser
|
|
XM_006718454.2:c.1468G>T
|
XP_006718517.1:p.Ala490Ser
|
|
XM_006718456.2:c.1468G>T
|
XP_006718519.1:p.Ala490Ser
|
|
XM_011544802.1:c.1228G>T
|
XP_011543104.1:p.Ala410Ser
|
|
XM_011544803.1:c.1468G>T
|
XP_011543105.1:p.Ala490Ser
|
|
XM_011544804.1:c.1468G>T
|
XP_011543106.1:p.Ala490Ser
|
|
XM_011544805.1:c.1468G>T
|
XP_011543107.1:p.Ala490Ser
|
|
XM_011544806.1:c.1468G>T
|
XP_011543108.1:p.Ala490Ser
|
|
XM_011544807.1:c.772G>T
|
XP_011543109.1:p.Ala258Ser
|
|
XM_011544808.1:c.637G>T
|
XP_011543110.1:p.Ala213Ser
|
|
XR_247191.1:n.1569G>T
|
|
|
XM_005273824.4:c.1465G>T
|
XP_005273881.1:p.Ala489Ser
|
|
XM_005273826.4:c.1213G>T
|
XP_005273883.1:p.Ala405Ser
|
|
XM_005273830.4:c.775G>T
|
XP_005273887.1:p.Ala259Ser
|
|
XM_005273831.4:c.775G>T
|
XP_005273888.1:p.Ala259Ser
|
|
XM_005273832.4:c.745G>T
|
XP_005273889.1:p.Ala249Ser
|
|
XM_011544802.3:c.1228G>T
|
XP_011543104.1:p.Ala410Ser
|
|
XM_011544807.3:c.772G>T
|
XP_011543109.1:p.Ala258Ser
|
|
XM_011544808.3:c.637G>T
|
XP_011543110.1:p.Ala213Ser
|
|
XM_017017328.2:c.1299G>T
|
XP_016872817.1:p.Leu433Phe
|
|
XM_017017329.2:c.1296G>T
|
XP_016872818.1:p.Leu432Phe
|
|
XM_017017330.2:c.745G>T
|
XP_016872819.1:p.Ala249Ser
|
|
XM_017017331.2:c.745G>T
|
XP_016872820.1:p.Ala249Ser
|
|
XM_017017332.2:c.559G>T
|
XP_016872821.1:p.Ala187Ser
|
|
XM_017017333.2:c.576G>T
|
XP_016872822.1:p.Leu192Phe
|
|
XM_017017334.2:c.576G>T
|
XP_016872823.1:p.Leu192Phe
|
|
XM_017017335.2:c.576G>T
|
XP_016872824.1:p.Leu192Phe
|
|
XM_017017336.2:c.468G>T
|
XP_016872825.1:p.Leu156Phe
|
|
XM_024448392.1:c.1258G>T
|
XP_024304160.1:p.Ala420Ser
|
|
XM_024448393.1:c.745G>T
|
XP_024304161.1:p.Ala249Ser
|
|
XR_001747789.2:n.1400G>T
|
|
|
XR_001747790.2:n.1400G>T
|
|
|
XR_247191.3:n.1572G>T
|
|
|
NM_139075.4:c.1468G>T
MANE Select
|
NP_620714.2:p.Ala490Ser
|
|