ENST00000593135.6:c.2511G>T
MANE Select
|
ENSP00000465992.1:p.Arg837Ser
|
|
ENST00000587309.5:c.*272G>T
|
ENSP00000465377.1:n.*272G>T
|
|
ENST00000593135.5:c.2511G>T
|
ENSP00000465992.1:p.Arg837Ser
|
|
NM_001264573.1:c.*272G>T
|
NP_001251503.1:n.*272G>T
|
|
NM_001265577.1:c.2511G>T
|
NP_001252506.1:p.Arg837Ser
|
|
XM_011524385.1:c.2574G>T
|
XP_011522687.1:p.Arg858Ser
|
|
XM_011524386.1:c.2547G>T
|
XP_011522688.1:p.Arg849Ser
|
|
XM_011524387.1:c.2547G>T
|
XP_011522689.1:p.Arg849Ser
|
|
XM_011524388.1:c.2538G>T
|
XP_011522690.1:p.Arg846Ser
|
|
XM_011524389.1:c.*272G>T
|
XP_011522691.1:n.*272G>T
|
|
XM_011524390.1:c.2469G>T
|
XP_011522692.1:p.Arg823Ser
|
|
XM_011524385.2:c.2574G>T
|
XP_011522687.1:p.Arg858Ser
|
|
XM_011524386.2:c.2547G>T
|
XP_011522688.1:p.Arg849Ser
|
|
XM_011524387.2:c.2547G>T
|
XP_011522689.1:p.Arg849Ser
|
|
XM_011524388.3:c.2538G>T
|
XP_011522690.1:p.Arg846Ser
|
|
XM_011524389.2:c.*272G>T
|
XP_011522691.1:n.*272G>T
|
|
XM_011524390.2:c.2469G>T
|
XP_011522692.1:p.Arg823Ser
|
|
NM_001264573.2:c.*272G>T
|
NP_001251503.1:n.*272G>T
|
|
NM_001265577.2:c.2511G>T
MANE Select
|
NP_001252506.1:p.Arg837Ser
|
|