ENST00000704350.1:c.3199G>T
|
ENSP00000515861.1:p.Ala1067Ser
|
|
ENST00000704352.1:c.1174-45762G>T
|
ENSP00000515863.1:n.1174-45762G>T
|
|
ENST00000704353.1:c.1174-45762G>T
|
ENSP00000515864.1:n.1174-45762G>T
|
|
ENST00000704354.1:c.3543G>T
|
|
|
ENST00000704355.1:c.1923G>T
|
|
|
ENST00000349721.8:c.3559G>T
MANE Select
|
ENSP00000265773.5:p.Ala1187Ser
|
|
ENST00000357248.8:c.3559G>T
|
ENSP00000349788.2:p.Ala1187Ser
|
|
ENST00000635739.1:n.2227G>T
|
|
|
ENST00000636157.1:n.1166G>T
|
|
|
ENST00000638139.1:n.593G>T
|
|
|
ENST00000349721.7:c.3559G>T
|
ENSP00000265773.5:p.Ala1187Ser
|
|
ENST00000357248.7:c.3559G>T
|
ENSP00000349788.2:p.Ala1187Ser
|
|
ENST00000382194.6:c.3559G>T
|
ENSP00000371629.1:p.Ala1187Ser
|
|
ENST00000382203.5:c.3559G>T
|
ENSP00000371638.1:p.Ala1187Ser
|
|
ENST00000450198.6:c.3385G>T
|
ENSP00000392081.2:p.Ala1129Ser
|
|
ENST00000634760.1:c.3559G>T
|
ENSP00000489256.1:p.Ala1187Ser
|
|
ENST00000634772.1:c.62-3534G>T
|
|
|
ENST00000634925.1:n.1050G>T
|
|
|
NM_001289396.1:c.3559G>T
|
NP_001276325.1:p.Ala1187Ser
|
|
NM_001289397.1:c.3385G>T
|
NP_001276326.1:p.Ala1129Ser
|
|
NM_003070.4:c.3559G>T
|
NP_003061.3:p.Ala1187Ser
|
|
NM_139045.3:c.3559G>T
|
NP_620614.2:p.Ala1187Ser
|
|
NM_003070.5:c.3559G>T
MANE Select
|
NP_003061.3:p.Ala1187Ser
|
|
NM_001289397.2:c.3385G>T
|
NP_001276326.1:p.Ala1129Ser
|
|
NM_139045.4:c.3559G>T
|
NP_620614.2:p.Ala1187Ser
|
|