ENST00000350051.8:c.423G>C
MANE Select
|
ENSP00000324180.4:p.Met141Ile
|
|
ENST00000301633.8:c.492G>C
|
ENSP00000301633.3:p.Met164Ile
|
|
ENST00000350051.7:c.423G>C
|
ENSP00000324180.4:p.Met141Ile
|
|
ENST00000374948.6:c.305G>C
|
ENSP00000364086.1:p.Trp102Ser
|
|
ENST00000589892.1:n.439G>C
|
|
|
ENST00000590925.6:c.*225G>C
|
ENSP00000467336.1:n.*225G>C
|
|
NM_001012270.1:c.305G>C
|
NP_001012270.1:p.Trp102Ser
|
|
NM_001012271.1:c.492G>C
|
NP_001012271.1:p.Met164Ile
|
|
NM_001168.2:c.423G>C
|
NP_001159.2:p.Met141Ile
|
|
XR_243654.3:n.625G>C
|
|
|
XR_934452.1:n.694G>C
|
|
|
XR_243654.5:n.625G>C
|
|
|
XR_934452.3:n.694G>C
|
|
|
NM_001168.3:c.423G>C
MANE Select
|
NP_001159.2:p.Met141Ile
|
|
NM_001012270.2:c.305G>C
|
NP_001012270.1:p.Trp102Ser
|
|
NM_001012271.2:c.492G>C
|
NP_001012271.1:p.Met164Ile
|
|