ENST00000389857.11:c.4663T>G
MANE Select
|
ENSP00000374507.6:p.Ser1555Ala
|
|
ENST00000331194.8:c.235T>G
|
ENSP00000330332.8:p.Ser79Ala
|
|
ENST00000334448.5:n.328T>G
|
|
|
ENST00000389857.10:c.4663T>G
|
ENSP00000374507.6:p.Ser1555Ala
|
|
ENST00000556726.5:c.891T>G
|
|
|
NM_001080414.3:c.4663T>G
|
NP_001073883.2:p.Ser1555Ala
|
|
XM_011536796.1:c.4555T>G
|
XP_011535098.1:p.Ser1519Ala
|
|
XR_429316.2:n.4791T>G
|
|
|
XR_943459.1:n.4791T>G
|
|
|
XM_011536796.2:c.4555T>G
|
XP_011535098.1:p.Ser1519Ala
|
|
XM_017021335.2:c.4663T>G
|
XP_016876824.1:p.Ser1555Ala
|
|
XM_017021336.1:c.1744T>G
|
XP_016876825.1:p.Ser582Ala
|
|
XR_429316.4:n.4789T>G
|
|
|
NM_001080414.4:c.4663T>G
MANE Select
|
NP_001073883.2:p.Ser1555Ala
|
|