ENST00000704350.1:c.3198G>T
|
ENSP00000515861.1:p.Ala1066=
|
|
ENST00000704352.1:c.1174-45763G>T
|
ENSP00000515863.1:n.1174-45763G>T
|
|
ENST00000704353.1:c.1174-45763G>T
|
ENSP00000515864.1:n.1174-45763G>T
|
|
ENST00000704354.1:c.3542G>T
|
|
|
ENST00000704355.1:c.1922G>T
|
|
|
ENST00000349721.8:c.3558G>T
MANE Select
|
ENSP00000265773.5:p.Ala1186=
|
|
ENST00000357248.8:c.3558G>T
|
ENSP00000349788.2:p.Ala1186=
|
|
ENST00000635739.1:n.2226G>T
|
|
|
ENST00000636157.1:n.1165G>T
|
|
|
ENST00000638139.1:n.592G>T
|
|
|
ENST00000349721.7:c.3558G>T
|
ENSP00000265773.5:p.Ala1186=
|
|
ENST00000357248.7:c.3558G>T
|
ENSP00000349788.2:p.Ala1186=
|
|
ENST00000382194.6:c.3558G>T
|
ENSP00000371629.1:p.Ala1186=
|
|
ENST00000382203.5:c.3558G>T
|
ENSP00000371638.1:p.Ala1186=
|
|
ENST00000450198.6:c.3384G>T
|
ENSP00000392081.2:p.Ala1128=
|
|
ENST00000634760.1:c.3558G>T
|
ENSP00000489256.1:p.Ala1186=
|
|
ENST00000634772.1:c.62-3535G>T
|
|
|
ENST00000634925.1:n.1049G>T
|
|
|
NM_001289396.1:c.3558G>T
|
NP_001276325.1:p.Ala1186=
|
|
NM_001289397.1:c.3384G>T
|
NP_001276326.1:p.Ala1128=
|
|
NM_003070.4:c.3558G>T
|
NP_003061.3:p.Ala1186=
|
|
NM_139045.3:c.3558G>T
|
NP_620614.2:p.Ala1186=
|
|
NM_003070.5:c.3558G>T
MANE Select
|
NP_003061.3:p.Ala1186=
|
|
NM_001289397.2:c.3384G>T
|
NP_001276326.1:p.Ala1128=
|
|
NM_139045.4:c.3558G>T
|
NP_620614.2:p.Ala1186=
|
|