ENST00000373207.2:c.3059C>T
MANE Select
|
ENSP00000362303.1:p.Ala1020Val
|
|
ENST00000373207.1:c.3059C>T
|
ENSP00000362303.1:p.Ala1020Val
|
|
ENST00000373208.5:c.3068C>T
|
ENSP00000362304.1:p.Ala1023Val
|
|
NM_080722.3:c.3059C>T
|
NP_542453.2:p.Ala1020Val
|
|
NM_139155.2:c.3068C>T
|
NP_631894.2:p.Ala1023Val
|
|
XM_011539300.1:c.2558C>T
|
XP_011537602.1:p.Ala853Val
|
|
XM_011539301.1:c.2132C>T
|
XP_011537603.1:p.Ala711Val
|
|
XM_011539302.1:c.2132C>T
|
XP_011537604.1:p.Ala711Val
|
|
XM_011539309.1:c.1628C>T
|
XP_011537611.1:p.Ala543Val
|
|
NM_080722.4:c.3059C>T
MANE Select
|
NP_542453.2:p.Ala1020Val
|
|
NM_139155.3:c.3068C>T
|
NP_631894.2:p.Ala1023Val
|
|
XM_011539300.2:c.2558C>T
|
XP_011537602.1:p.Ala853Val
|
|
XM_011539301.2:c.2132C>T
|
XP_011537603.1:p.Ala711Val
|
|
XM_011539302.2:c.2132C>T
|
XP_011537604.1:p.Ala711Val
|
|