ENST00000455146.8:c.303T>C
MANE Select
|
ENSP00000397441.2:p.Leu101=
|
|
ENST00000356576.8:c.*140T>C
|
ENSP00000348983.4:n.*140T>C
|
|
ENST00000416691.5:c.303T>C
|
ENSP00000403733.1:p.Leu101=
|
|
ENST00000422759.6:n.368T>C
|
|
|
ENST00000455146.7:c.303T>C
|
ENSP00000397441.2:p.Leu101=
|
|
ENST00000536488.5:c.118T>C
|
|
|
ENST00000543804.5:c.*64T>C
|
ENSP00000440473.1:n.*64T>C
|
|
NM_001145079.1:c.303T>C
|
NP_001138551.1:p.Leu101=
|
|
NM_020751.2:c.303T>C
|
NP_065802.1:p.Leu101=
|
|
NR_026745.1:n.468T>C
|
|
|
XM_011535168.1:c.303T>C
|
XP_011533470.1:p.Leu101=
|
|
XM_011535169.1:c.147T>C
|
XP_011533471.1:p.Leu49=
|
|
XM_011535170.1:c.147T>C
|
XP_011533472.1:p.Leu49=
|
|
NM_020751.3:c.303T>C
MANE Select
|
NP_065802.1:p.Leu101=
|
|
NM_001145079.2:c.303T>C
|
NP_001138551.1:p.Leu101=
|
|