ENST00000409013.8:c.612G>C
MANE Select
|
ENSP00000387139.3:p.Ala204=
|
|
ENST00000315658.11:c.612G>C
|
ENSP00000318264.7:p.Ala204=
|
|
ENST00000393852.8:c.612G>C
|
ENSP00000377434.4:p.Ala204=
|
|
ENST00000409013.7:c.612G>C
|
ENSP00000387139.3:p.Ala204=
|
|
ENST00000409344.7:c.612G>C
|
ENSP00000386248.3:p.Ala204=
|
|
ENST00000409890.6:c.612G>C
|
ENSP00000386304.2:p.Ala204=
|
|
ENST00000410106.5:c.*284G>C
|
ENSP00000387134.1:n.*284G>C
|
|
ENST00000414593.5:c.*3G>C
|
ENSP00000394774.1:n.*3G>C
|
|
ENST00000423095.7:c.484+6139G>C
|
ENSP00000408745.3:n.484+6139G>C
|
|
ENST00000429764.5:c.*3G>C
|
ENSP00000408329.1:n.*3G>C
|
|
ENST00000444108.7:c.612G>C
|
ENSP00000401984.2:p.Ala204=
|
|
ENST00000446464.7:c.612G>C
|
ENSP00000407599.3:p.Ala204=
|
|
ENST00000490508.5:n.824G>C
|
|
|
ENST00000496957.1:n.40G>C
|
|
|
NM_001135021.1:c.612G>C
|
NP_001128493.1:p.Ala204=
|
|
NM_001135022.1:c.612G>C
|
NP_001128494.1:p.Ala204=
|
|
NM_001135023.1:c.612G>C
|
NP_001128495.1:p.Ala204=
|
|
NM_032213.4:c.612G>C
|
NP_115589.2:p.Ala204=
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|
XM_005264596.2:c.612G>C
|
XP_005264653.1:p.Ala204=
|
|
XM_005264597.2:c.612G>C
|
XP_005264654.1:p.Ala204=
|
|
XM_005264598.2:c.612G>C
|
XP_005264655.1:p.Ala204=
|
|
XM_006712116.1:c.612G>C
|
XP_006712179.1:p.Ala204=
|
|
XR_426997.1:n.763G>C
|
|
|
NM_001329791.1:c.612G>C
|
NP_001316720.1:p.Ala204=
|
|
NM_001329792.1:c.612G>C
|
NP_001316721.1:p.Ala204=
|
|
NM_001329793.1:c.612G>C
|
NP_001316722.1:p.Ala204=
|
|
NR_138131.1:n.1049G>C
|
|
|
NR_138132.1:n.1268G>C
|
|
|
NR_138133.1:n.831G>C
|
|
|
XM_024453169.1:c.612G>C
|
XP_024308937.1:p.Ala204=
|
|
XM_024453170.1:c.612G>C
|
XP_024308938.1:p.Ala204=
|
|
XM_024453171.1:c.612G>C
|
XP_024308939.1:p.Ala204=
|
|
XM_024453172.1:c.612G>C
|
XP_024308940.1:p.Ala204=
|
|
XR_001738978.1:n.1093G>C
|
|
|
XR_001738979.1:n.998G>C
|
|
|
NM_001135022.2:c.612G>C
MANE Select
|
NP_001128494.1:p.Ala204=
|
|
NM_001135021.2:c.612G>C
|
NP_001128493.1:p.Ala204=
|
|
NM_001135023.2:c.612G>C
|
NP_001128495.1:p.Ala204=
|
|
NM_001329791.2:c.612G>C
|
NP_001316720.1:p.Ala204=
|
|
NM_001329792.2:c.612G>C
|
NP_001316721.1:p.Ala204=
|
|
NM_001329793.2:c.612G>C
|
NP_001316722.1:p.Ala204=
|
|
NR_138131.2:n.1000G>C
|
|
|
NR_138132.2:n.1219G>C
|
|
|
NR_138133.2:n.782G>C
|
|
|