ENST00000261978.9:c.5371G>C
MANE Select
|
ENSP00000261978.4:p.Gly1791Arg
|
|
ENST00000261978.8:c.5371G>C
|
ENSP00000261978.4:p.Gly1791Arg
|
|
ENST00000553939.5:c.*150G>C
|
ENSP00000452110.1:n.*150G>C
|
|
ENST00000554861.1:n.589G>C
|
|
|
ENST00000556690.5:c.5239G>C
|
ENSP00000451477.1:p.Gly1747Arg
|
|
NM_000428.2:c.5371G>C
|
NP_000419.1:p.Gly1791Arg
|
|
XM_011536765.1:c.4990G>C
|
XP_011535067.1:p.Gly1664Arg
|
|
XM_011536766.1:c.4912G>C
|
XP_011535068.1:p.Gly1638Arg
|
|
XM_011536767.1:c.4888G>C
|
XP_011535069.1:p.Gly1630Arg
|
|
XM_011536765.2:c.4990G>C
|
XP_011535067.1:p.Gly1664Arg
|
|
NM_000428.3:c.5371G>C
MANE Select
|
NP_000419.1:p.Gly1791Arg
|
|