ENST00000220616.9:c.6764G>T
MANE Select
|
ENSP00000220616.4:p.Trp2255Leu
|
|
ENST00000220616.8:c.6764G>T
|
ENSP00000220616.4:p.Trp2255Leu
|
|
ENST00000518108.1:c.168+113G>T
|
|
|
ENST00000519178.5:c.2130G>T
|
|
|
ENST00000519543.5:c.1163G>T
|
ENSP00000430430.1:p.Trp388Leu
|
|
ENST00000523756.5:c.3419G>T
|
|
|
NM_003235.4:c.6764G>T
|
NP_003226.4:p.Trp2255Leu
|
|
XM_005251038.3:c.6572G>T
|
XP_005251095.1:p.Trp2191Leu
|
|
XM_006716622.2:c.6701G>T
|
XP_006716685.1:p.Trp2234Leu
|
|
XM_005251038.4:c.6572G>T
|
XP_005251095.1:p.Trp2191Leu
|
|
XM_006716622.3:c.6701G>T
|
XP_006716685.1:p.Trp2234Leu
|
|
XM_017013793.1:c.6698G>T
|
XP_016869282.1:p.Trp2233Leu
|
|
XM_017013794.1:c.6764G>T
|
XP_016869283.1:p.Trp2255Leu
|
|
XM_017013795.1:c.6593G>T
|
XP_016869284.1:p.Trp2198Leu
|
|
XM_017013796.1:c.6545G>T
|
XP_016869285.1:p.Trp2182Leu
|
|
XM_017013797.1:c.6503G>T
|
XP_016869286.1:p.Trp2168Leu
|
|
XM_017013798.1:c.6764G>T
|
XP_016869287.1:p.Trp2255Leu
|
|
NM_003235.5:c.6764G>T
MANE Select
|
NP_003226.4:p.Trp2255Leu
|
|