ENST00000695527.1:n.112C>T
|
|
|
ENST00000695558.1:c.5800C>T
|
ENSP00000512015.1:p.Arg1934Ter
|
|
ENST00000703224.1:c.*5010C>T
|
ENSP00000515242.1:n.*5010C>T
|
|
ENST00000359568.10:c.5767C>T
MANE Select
|
ENSP00000352572.5:p.Arg1923Ter
|
|
ENST00000359568.9:c.5767C>T
|
ENSP00000352572.5:p.Arg1923Ter
|
|
ENST00000480896.5:n.6036C>T
|
|
|
NM_001315529.1:c.5413C>T
|
NP_001302458.1:p.Arg1805Ter
|
|
NM_006031.5:c.5767C>T
|
NP_006022.3:p.Arg1923Ter
|
|
XM_005261124.3:c.5800C>T
|
XP_005261181.1:p.Arg1934Ter
|
|
XM_011529593.1:c.5878C>T
|
XP_011527895.1:p.Arg1960Ter
|
|
XM_011529594.1:c.5848C>T
|
XP_011527896.1:p.Arg1950Ter
|
|
XM_005261124.5:c.5800C>T
|
XP_005261181.1:p.Arg1934Ter
|
|
XM_011529594.3:c.5848C>T
|
XP_011527896.1:p.Arg1950Ter
|
|
XM_017028362.2:c.5767C>T
|
XP_016883851.1:p.Arg1923Ter
|
|
XM_017028363.1:c.5446C>T
|
XP_016883852.1:p.Arg1816Ter
|
|
XM_024452082.1:c.4684C>T
|
XP_024307850.1:p.Arg1562Ter
|
|
XM_024452083.1:c.3580C>T
|
XP_024307851.1:p.Arg1194Ter
|
|
NM_006031.6:c.5767C>T
MANE Select
|
NP_006022.3:p.Arg1923Ter
|
|
NM_001315529.2:c.5413C>T
|
NP_001302458.1:p.Arg1805Ter
|
|