ENST00000237596.7:c.1511G>T
MANE Select
|
ENSP00000237596.2:p.Arg504Met
|
|
ENST00000237596.6:c.1511G>T
|
ENSP00000237596.2:p.Arg504Met
|
|
ENST00000508588.5:c.-199+3376G>T
|
ENSP00000427131.1:n.-199+3376G>T
|
|
NM_000297.3:c.1511G>T
|
NP_000288.1:p.Arg504Met
|
|
XM_011532028.1:c.1286G>T
|
XP_011530330.1:p.Arg429Met
|
|
XM_011532029.1:c.791G>T
|
XP_011530331.1:p.Arg264Met
|
|
XM_011532030.1:c.671G>T
|
XP_011530332.1:p.Arg224Met
|
|
XR_244632.2:n.1606G>T
|
|
|
NR_156488.1:n.1598G>T
|
|
|
XM_011532028.2:c.1286G>T
|
XP_011530330.1:p.Arg429Met
|
|
XM_011532030.2:c.671G>T
|
XP_011530332.1:p.Arg224Met
|
|
NM_000297.4:c.1511G>T
MANE Select
|
NP_000288.1:p.Arg504Met
|
|
NR_156488.2:n.1610G>T
|
|
|