ENST00000376883.2:c.1369G>T
MANE Select
|
ENSP00000366080.2:p.Asp457Tyr
|
|
ENST00000488757.6:c.1153G>T
|
ENSP00000418259.2:p.Asp385Tyr
|
|
ENST00000376881.4:c.1117G>T
|
ENSP00000366078.4:p.Asp373Tyr
|
|
ENST00000376883.1:c.1309G>T
|
ENSP00000366080.1:p.Asp437Tyr
|
|
ENST00000488757.5:c.1369G>T
|
ENSP00000418259.1:p.Asp457Tyr
|
|
NM_001109809.2:c.1369G>T
|
NP_001103279.2:p.Asp457Tyr
|
|
XM_006715087.2:c.1153G>T
|
XP_006715150.1:p.Asp385Tyr
|
|
XM_011514570.1:c.1369G>T
|
XP_011512872.1:p.Asp457Tyr
|
|
NM_001109809.3:c.1369G>T
|
NP_001103279.2:p.Asp457Tyr
|
|
NM_001366333.1:c.1153G>T
|
NP_001353262.1:p.Asp385Tyr
|
|
NM_001109809.4:c.1369G>T
|
NP_001103279.2:p.Asp457Tyr
|
|
NM_001366333.2:c.1153G>T
|
NP_001353262.1:p.Asp385Tyr
|
|
NM_001109809.5:c.1369G>T
MANE Select
|
NP_001103279.2:p.Asp457Tyr
|
|