|
NM_015202.5:c.1672C>T
MANE Select
|
NP_056017.4:p.Arg558Ter
|
|
ENST00000261588.10:c.1672C>T
MANE Select
|
ENSP00000261588.4:p.Arg558Ter
|
|
NM_015202.2:c.1672C>T
|
NP_056017.2:p.Arg558Ter
|
|
NM_015202.3:c.1672C>T
|
NP_056017.3:p.Arg558Ter
|
|
NM_015202.4:c.1672C>T
|
NP_056017.3:p.Arg558Ter
|
|
ENST00000261588.8:c.1672C>T
|
ENSP00000261588.4:p.Arg558Ter
|
|
ENST00000261588.9:c.1672C>T
|
ENSP00000261588.4:p.Arg558Ter
|
|
ENST00000567894.5:n.1533C>T
|
|
|
ENST00000573850.1:n.657C>T
|
|
|
XM_005255201.2:c.1855C>T
|
XP_005255258.1:p.Arg619Ter
|
|
XM_005255201.3:c.1855C>T
|
XP_005255258.1:p.Arg619Ter
|
|
XM_005255202.2:c.1801C>T
|
XP_005255259.1:p.Arg601Ter
|
|
XM_005255202.3:c.1801C>T
|
XP_005255259.1:p.Arg601Ter
|
|
XM_005255203.2:c.1726C>T
|
XP_005255260.1:p.Arg576Ter
|
|
XM_005255203.3:c.1726C>T
|
XP_005255260.1:p.Arg576Ter
|
|
XM_005255206.2:c.1855C>T
|
XP_005255263.1:p.Arg619Ter
|
|
XM_005255206.3:c.1855C>T
|
XP_005255263.1:p.Arg619Ter
|
|
XM_005255207.2:c.550C>T
|
XP_005255264.1:p.Arg184Ter
|
|
XM_005255208.2:c.451C>T
|
XP_005255265.1:p.Arg151Ter
|
|
XM_006721025.2:c.1594C>T
|
XP_006721088.1:p.Arg532Ter
|
|
XM_006721025.3:c.1594C>T
|
XP_006721088.1:p.Arg532Ter
|
|
XM_011545773.1:c.1777C>T
|
XP_011544075.1:p.Arg593Ter
|
|
XM_011545773.2:c.1777C>T
|
XP_011544075.1:p.Arg593Ter
|
|
XM_011545774.1:c.1777C>T
|
XP_011544076.1:p.Arg593Ter
|
|
XM_011545774.2:c.1777C>T
|
XP_011544076.1:p.Arg593Ter
|
|
XM_011545775.1:c.1735C>T
|
XP_011544077.1:p.Arg579Ter
|
|
XM_011545775.2:c.1735C>T
|
XP_011544077.1:p.Arg579Ter
|
|
XM_011545776.1:c.1723C>T
|
XP_011544078.1:p.Arg575Ter
|
|
XM_011545776.2:c.1723C>T
|
XP_011544078.1:p.Arg575Ter
|
|
XM_017023085.1:c.1606C>T
|
XP_016878574.1:p.Arg536Ter
|
|
XM_017023086.1:c.1594C>T
|
XP_016878575.1:p.Arg532Ter
|
|
XM_017023087.1:c.1540C>T
|
XP_016878576.1:p.Arg514Ter
|
|
XM_017023088.1:c.550C>T
|
XP_016878577.1:p.Arg184Ter
|
|
XM_024450216.1:c.1669C>T
|
XP_024305984.1:p.Arg557Ter
|
|
XM_024450217.1:c.1189C>T
|
XP_024305985.1:p.Arg397Ter
|
