ENST00000704350.1:c.3196G=
|
ENSP00000515861.1:p.Ala1066=
|
|
ENST00000704352.1:c.1174-45765G=
|
ENSP00000515863.1:n.1174-45765G=
|
|
ENST00000704353.1:c.1174-45765G=
|
ENSP00000515864.1:n.1174-45765G=
|
|
ENST00000704354.1:c.3540G=
|
|
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ENST00000704355.1:c.1920G=
|
|
|
ENST00000349721.8:c.3556G=
MANE Select
|
ENSP00000265773.5:p.Ala1186=
|
|
ENST00000357248.8:c.3556G=
|
ENSP00000349788.2:p.Ala1186=
|
|
ENST00000635739.1:n.2224G=
|
|
|
ENST00000636157.1:n.1163G=
|
|
|
ENST00000638139.1:n.590G=
|
|
|
ENST00000349721.7:c.3556G=
|
ENSP00000265773.5:p.Ala1186=
|
|
ENST00000357248.7:c.3556G=
|
ENSP00000349788.2:p.Ala1186=
|
|
ENST00000382194.6:c.3556G=
|
ENSP00000371629.1:p.Ala1186=
|
|
ENST00000382203.5:c.3556G=
|
ENSP00000371638.1:p.Ala1186=
|
|
ENST00000450198.6:c.3382G=
|
ENSP00000392081.2:p.Ala1128=
|
|
ENST00000634760.1:c.3556G=
|
ENSP00000489256.1:p.Ala1186=
|
|
ENST00000634772.1:c.62-3537G=
|
|
|
ENST00000634925.1:n.1047G=
|
|
|
NM_001289396.1:c.3556G=
|
NP_001276325.1:p.Ala1186=
|
|
NM_001289397.1:c.3382G=
|
NP_001276326.1:p.Ala1128=
|
|
NM_003070.4:c.3556G=
|
NP_003061.3:p.Ala1186=
|
|
NM_139045.3:c.3556G=
|
NP_620614.2:p.Ala1186=
|
|
NM_003070.5:c.3556G=
MANE Select
|
NP_003061.3:p.Ala1186=
|
|
NM_001289397.2:c.3382G=
|
NP_001276326.1:p.Ala1128=
|
|
NM_139045.4:c.3556G=
|
NP_620614.2:p.Ala1186=
|
|