ENST00000379370.7:c.3922C>T
MANE Select
|
ENSP00000368678.2:p.Arg1308Cys
|
|
ENST00000651234.1:c.3607C>T
|
ENSP00000499046.1:p.Arg1203Cys
|
|
ENST00000652369.1:c.3607C>T
|
ENSP00000498543.1:p.Arg1203Cys
|
|
ENST00000379370.6:c.3922C>T
|
ENSP00000368678.2:p.Arg1308Cys
|
|
ENST00000620552.4:c.3508C>T
|
ENSP00000484607.1:p.Arg1170Cys
|
|
NM_001305275.1:c.3922C>T
|
NP_001292204.1:p.Arg1308Cys
|
|
NM_198576.3:c.3922C>T
|
NP_940978.2:p.Arg1308Cys
|
|
XM_005244749.2:c.3922C>T
|
XP_005244806.1:p.Arg1308Cys
|
|
XM_006710635.2:c.3922C>T
|
XP_006710698.1:p.Arg1308Cys
|
|
XM_011541429.1:c.3922C>T
|
XP_011539731.1:p.Arg1308Cys
|
|
XM_011541430.1:c.3049C>T
|
XP_011539732.1:p.Arg1017Cys
|
|
XM_011541431.1:c.2188C>T
|
XP_011539733.1:p.Arg730Cys
|
|
XR_946650.1:n.3989C>T
|
|
|
NM_001364727.1:c.3607C>T
|
NP_001351656.1:p.Arg1203Cys
|
|
XM_005244749.3:c.3922C>T
|
XP_005244806.1:p.Arg1308Cys
|
|
XM_011541429.2:c.3922C>T
|
XP_011539731.1:p.Arg1308Cys
|
|
XR_946650.2:n.3993C>T
|
|
|
NM_001305275.2:c.3922C>T
|
NP_001292204.1:p.Arg1308Cys
|
|
NM_198576.4:c.3922C>T
MANE Select
|
NP_940978.2:p.Arg1308Cys
|
|
NM_001364727.2:c.3607C>T
|
NP_001351656.1:p.Arg1203Cys
|
|