ENST00000237596.7:c.2230G>T
MANE Select
|
ENSP00000237596.2:p.Asp744Tyr
|
|
ENST00000237596.6:c.2230G>T
|
ENSP00000237596.2:p.Asp744Tyr
|
|
ENST00000502363.1:c.484G>T
|
ENSP00000425289.1:p.Asp162Tyr
|
|
ENST00000508588.5:c.484G>T
|
ENSP00000427131.1:p.Asp162Tyr
|
|
ENST00000511337.5:n.482G>T
|
|
|
ENST00000512858.1:n.442G>T
|
|
|
NM_000297.3:c.2230G>T
|
NP_000288.1:p.Asp744Tyr
|
|
XM_011532028.1:c.2005G>T
|
XP_011530330.1:p.Asp669Tyr
|
|
XM_011532029.1:c.1510G>T
|
XP_011530331.1:p.Asp504Tyr
|
|
XM_011532030.1:c.1390G>T
|
XP_011530332.1:p.Asp464Tyr
|
|
NR_156488.1:n.2196G>T
|
|
|
XM_011532028.2:c.2005G>T
|
XP_011530330.1:p.Asp669Tyr
|
|
XM_011532030.2:c.1390G>T
|
XP_011530332.1:p.Asp464Tyr
|
|
NM_000297.4:c.2230G>T
MANE Select
|
NP_000288.1:p.Asp744Tyr
|
|
NR_156488.2:n.2208G>T
|
|
|