ENST00000220616.9:c.8140G>T
MANE Select
|
ENSP00000220616.4:p.Asp2714Tyr
|
|
ENST00000220616.8:c.8140G>T
|
ENSP00000220616.4:p.Asp2714Tyr
|
|
ENST00000519178.5:c.3506G>T
|
|
|
ENST00000519543.5:c.2539G>T
|
ENSP00000430430.1:p.Asp847Tyr
|
|
ENST00000521107.1:c.352G>T
|
ENSP00000430161.1:p.Asp118Tyr
|
|
ENST00000522691.1:n.226G>T
|
|
|
ENST00000523756.5:c.4795G>T
|
|
|
NM_003235.4:c.8140G>T
|
NP_003226.4:p.Asp2714Tyr
|
|
XM_005251038.3:c.7948G>T
|
XP_005251095.1:p.Asp2650Tyr
|
|
XM_006716622.2:c.8077G>T
|
XP_006716685.1:p.Asp2693Tyr
|
|
XM_005251038.4:c.7948G>T
|
XP_005251095.1:p.Asp2650Tyr
|
|
XM_006716622.3:c.8077G>T
|
XP_006716685.1:p.Asp2693Tyr
|
|
XM_017013793.1:c.8074G>T
|
XP_016869282.1:p.Asp2692Tyr
|
|
XM_017013794.1:c.8005G>T
|
XP_016869283.1:p.Asp2669Tyr
|
|
XM_017013795.1:c.7969G>T
|
XP_016869284.1:p.Asp2657Tyr
|
|
XM_017013796.1:c.7921G>T
|
XP_016869285.1:p.Asp2641Tyr
|
|
XM_017013797.1:c.7879G>T
|
XP_016869286.1:p.Asp2627Tyr
|
|
NM_003235.5:c.8140G>T
MANE Select
|
NP_003226.4:p.Asp2714Tyr
|
|