ENST00000383788.10:c.386G>C
MANE Select
|
ENSP00000373298.3:p.Gly129Ala
|
|
ENST00000679838.1:c.*148G>C
|
ENSP00000505708.1:n.*148G>C
|
|
ENST00000681097.1:c.386G>C
|
ENSP00000505397.1:p.Gly129Ala
|
|
ENST00000383781.8:c.356G>C
|
ENSP00000373291.3:p.Gly119Ala
|
|
ENST00000383786.9:c.284G>C
|
ENSP00000373296.3:p.Gly95Ala
|
|
ENST00000383788.9:c.386G>C
|
ENSP00000373298.3:p.Gly129Ala
|
|
ENST00000603469.1:n.57G>C
|
|
|
ENST00000603808.5:c.386G>C
|
ENSP00000474271.1:p.Gly129Ala
|
|
ENST00000605797.1:c.215G>C
|
ENSP00000474936.1:p.Gly72Ala
|
|
NM_005677.3:c.386G>C
|
NP_005668.2:p.Gly129Ala
|
|
NM_080538.2:c.356G>C
|
NP_536799.1:p.Gly119Ala
|
|
NM_080539.3:c.284G>C
|
NP_536800.2:p.Gly95Ala
|
|
NM_005677.4:c.386G>C
MANE Select
|
NP_005668.2:p.Gly129Ala
|
|
NM_080539.4:c.284G>C
|
NP_536800.2:p.Gly95Ala
|
|