ENST00000312428.11:c.10745T>G
MANE Select
|
ENSP00000311273.6:p.Leu3582Arg
|
|
ENST00000312428.10:c.10745T>G
|
ENSP00000311273.6:p.Leu3582Arg
|
|
ENST00000409063.5:c.194T>G
|
ENSP00000386912.1:p.Leu65Arg
|
|
NM_018897.2:c.10745T>G
|
NP_061720.2:p.Leu3582Arg
|
|
XM_011511487.1:c.10745T>G
|
XP_011509789.1:p.Leu3582Arg
|
|
XM_011511488.1:c.10625T>G
|
XP_011509790.1:p.Leu3542Arg
|
|
XM_011511489.1:c.10607T>G
|
XP_011509791.1:p.Leu3536Arg
|
|
XM_011511490.1:c.10520T>G
|
XP_011509792.1:p.Leu3507Arg
|
|
XM_011511496.1:c.6389T>G
|
XP_011509798.1:p.Leu2130Arg
|
|
XM_011511497.1:c.5117T>G
|
XP_011509799.1:p.Leu1706Arg
|
|
XM_011511488.3:c.10625T>G
|
XP_011509790.1:p.Leu3542Arg
|
|
XM_011511489.2:c.10607T>G
|
XP_011509791.1:p.Leu3536Arg
|
|
XM_011511490.3:c.10520T>G
|
XP_011509792.1:p.Leu3507Arg
|
|
XM_011511497.2:c.5117T>G
|
XP_011509799.1:p.Leu1706Arg
|
|
XM_017004504.2:c.10472T>G
|
XP_016859993.1:p.Leu3491Arg
|
|
NM_018897.3:c.10745T>G
MANE Select
|
NP_061720.2:p.Leu3582Arg
|
|