ENST00000220616.9:c.8168C>G
MANE Select
|
ENSP00000220616.4:p.Ser2723Trp
|
|
ENST00000220616.8:c.8168C>G
|
ENSP00000220616.4:p.Ser2723Trp
|
|
ENST00000519178.5:c.3534C>G
|
|
|
ENST00000519543.5:c.2567C>G
|
ENSP00000430430.1:p.Ser856Trp
|
|
ENST00000521107.1:c.380C>G
|
ENSP00000430161.1:p.Ser127Trp
|
|
ENST00000522691.1:n.254C>G
|
|
|
ENST00000523756.5:c.4823C>G
|
|
|
NM_003235.4:c.8168C>G
|
NP_003226.4:p.Ser2723Trp
|
|
XM_005251038.3:c.7976C>G
|
XP_005251095.1:p.Ser2659Trp
|
|
XM_006716622.2:c.8105C>G
|
XP_006716685.1:p.Ser2702Trp
|
|
XM_005251038.4:c.7976C>G
|
XP_005251095.1:p.Ser2659Trp
|
|
XM_006716622.3:c.8105C>G
|
XP_006716685.1:p.Ser2702Trp
|
|
XM_017013793.1:c.8102C>G
|
XP_016869282.1:p.Ser2701Trp
|
|
XM_017013794.1:c.8033C>G
|
XP_016869283.1:p.Ser2678Trp
|
|
XM_017013795.1:c.7997C>G
|
XP_016869284.1:p.Ser2666Trp
|
|
XM_017013796.1:c.7949C>G
|
XP_016869285.1:p.Ser2650Trp
|
|
XM_017013797.1:c.7907C>G
|
XP_016869286.1:p.Ser2636Trp
|
|
NM_003235.5:c.8168C>G
MANE Select
|
NP_003226.4:p.Ser2723Trp
|
|