ENST00000379370.7:c.3713G>T
MANE Select
|
ENSP00000368678.2:p.Arg1238Met
|
|
ENST00000651234.1:c.3398G>T
|
ENSP00000499046.1:p.Arg1133Met
|
|
ENST00000652369.1:c.3398G>T
|
ENSP00000498543.1:p.Arg1133Met
|
|
ENST00000379370.6:c.3713G>T
|
ENSP00000368678.2:p.Arg1238Met
|
|
ENST00000466223.1:n.451G>T
|
|
|
ENST00000620552.4:c.3299G>T
|
ENSP00000484607.1:p.Arg1100Met
|
|
NM_001305275.1:c.3713G>T
|
NP_001292204.1:p.Arg1238Met
|
|
NM_198576.3:c.3713G>T
|
NP_940978.2:p.Arg1238Met
|
|
XM_005244749.2:c.3713G>T
|
XP_005244806.1:p.Arg1238Met
|
|
XM_006710635.2:c.3713G>T
|
XP_006710698.1:p.Arg1238Met
|
|
XM_011541429.1:c.3713G>T
|
XP_011539731.1:p.Arg1238Met
|
|
XM_011541430.1:c.2840G>T
|
XP_011539732.1:p.Arg947Met
|
|
XM_011541431.1:c.1979G>T
|
XP_011539733.1:p.Arg660Met
|
|
XR_946650.1:n.3780G>T
|
|
|
NM_001364727.1:c.3398G>T
|
NP_001351656.1:p.Arg1133Met
|
|
XM_005244749.3:c.3713G>T
|
XP_005244806.1:p.Arg1238Met
|
|
XM_011541429.2:c.3713G>T
|
XP_011539731.1:p.Arg1238Met
|
|
XR_946650.2:n.3784G>T
|
|
|
NM_001305275.2:c.3713G>T
|
NP_001292204.1:p.Arg1238Met
|
|
NM_198576.4:c.3713G>T
MANE Select
|
NP_940978.2:p.Arg1238Met
|
|
NM_001364727.2:c.3398G>T
|
NP_001351656.1:p.Arg1133Met
|
|