ENST00000234071.8:c.1062A>C
MANE Select
|
ENSP00000234071.4:p.Arg354Ser
|
|
ENST00000234071.7:c.1062A>C
|
ENSP00000234071.3:p.Arg354Ser
|
|
ENST00000402125.2:c.386A>C
|
|
|
ENST00000409048.1:c.1164A>C
|
ENSP00000386679.1:p.Arg388Ser
|
|
NM_000312.3:c.1062A>C , LRG_599t1:c.1062A>C
|
NP_000303.1:p.Arg354Ser
|
|
XM_005263715.3:c.1245A>C
|
XP_005263772.1:p.Arg415Ser
|
|
XM_005263716.3:c.1227A>C
|
XP_005263773.1:p.Arg409Ser
|
|
XM_005263717.3:c.1125A>C
|
XP_005263774.1:p.Arg375Ser
|
|
XR_923313.1:n.1332-358T>G
|
|
|
XM_005263717.4:c.1125A>C
|
XP_005263774.1:p.Arg375Ser
|
|
XM_017004505.1:c.1305A>C
|
XP_016859994.1:p.Arg435Ser
|
|
XM_024453002.1:c.1407A>C
|
XP_024308770.1:p.Arg469Ser
|
|
XM_024453003.1:c.1347A>C
|
XP_024308771.1:p.Arg449Ser
|
|
XM_024453004.1:c.1245A>C
|
XP_024308772.1:p.Arg415Ser
|
|
XM_024453005.1:c.1227A>C
|
XP_024308773.1:p.Arg409Ser
|
|
XM_024453006.1:c.1164A>C
|
XP_024308774.1:p.Arg388Ser
|
|
XR_001739705.1:n.3607-358T>G
|
|
|
XR_923313.2:n.4043-358T>G
|
|
|
NM_000312.4:c.1062A>C
MANE Select
|
NP_000303.1:p.Arg354Ser
|
|
NM_001375602.1:c.1245A>C
|
NP_001362531.1:p.Arg415Ser
|
|
NM_001375603.1:c.1227A>C
|
NP_001362532.1:p.Arg409Ser
|
|
NM_001375604.1:c.1125A>C
|
NP_001362533.1:p.Arg375Ser
|
|
NM_001375605.1:c.1164A>C
|
NP_001362534.1:p.Arg388Ser
|
|
NM_001375606.1:c.1230A>C
|
NP_001362535.1:p.Arg410Ser
|
|
NM_001375607.1:c.1248A>C
|
NP_001362536.1:p.Arg416Ser
|
|
NM_001375608.1:c.1005A>C
|
NP_001362537.1:p.Arg335Ser
|
|
NM_001375609.1:c.1038A>C
|
NP_001362538.1:p.Arg346Ser
|
|
NM_001375610.1:c.1056A>C
|
NP_001362539.1:p.Arg352Ser
|
|
NM_001375611.1:c.1062A>C
|
NP_001362540.1:p.Arg354Ser
|
|
NM_001375613.1:c.1062A>C
|
NP_001362542.1:p.Arg354Ser
|
|