ENST00000539276.7:c.1996C>T
MANE Select
|
ENSP00000440045.2:p.Arg666Ter
|
|
ENST00000308664.10:c.1996C>T
|
ENSP00000311186.6:p.Arg666Ter
|
|
ENST00000377685.9:c.*1836C>T
|
ENSP00000366913.4:n.*1836C>T
|
|
ENST00000539276.6:c.1996C>T
|
ENSP00000440045.2:p.Arg666Ter
|
|
ENST00000548169.2:c.1667C>T
|
|
|
NM_001681.3:c.1996C>T
|
NP_001672.1:p.Arg666Ter
|
|
NM_170665.3:c.1996C>T
|
NP_733765.1:p.Arg666Ter
|
|
XM_005253888.1:c.1996C>T
|
XP_005253945.1:p.Arg666Ter
|
|
XM_011538402.1:c.1996C>T
|
XP_011536704.1:p.Arg666Ter
|
|
XM_011538403.1:c.1996C>T
|
XP_011536705.1:p.Arg666Ter
|
|
XR_243009.1:n.2002C>T
|
|
|
XM_005253888.3:c.1996C>T
|
XP_005253945.1:p.Arg666Ter
|
|
XM_011538402.3:c.1996C>T
|
XP_011536704.1:p.Arg666Ter
|
|
XR_002957329.1:n.2002C>T
|
|
|
XR_243009.3:n.2002C>T
|
|
|
NM_170665.4:c.1996C>T
MANE Select
|
NP_733765.1:p.Arg666Ter
|
|
NM_001681.4:c.1996C>T
|
NP_001672.1:p.Arg666Ter
|
|