|
NM_001197104.2:c.3301C>T
MANE Select
|
NP_001184033.1:p.Arg1101Ter
|
|
ENST00000534358.8:c.3301C>T
MANE Select
|
ENSP00000436786.2:p.Arg1101Ter
|
|
NM_001197104.1:c.3301C>T , LRG_613t1:c.3301C>T
|
NP_001184033.1:p.Arg1101Ter
|
|
NM_005933.3:c.3301C>T
|
NP_005924.2:p.Arg1101Ter
|
|
NM_005933.4:c.3301C>T
|
NP_005924.2:p.Arg1101Ter
|
|
ENST00000389506.10:c.3301C>T
|
ENSP00000374157.5:p.Arg1101Ter
|
|
ENST00000389506.9:c.3301C>T
|
ENSP00000374157.5:p.Arg1101Ter
|
|
ENST00000527869.7:c.883C>T
|
ENSP00000432652.3:p.Arg295Ter
|
|
ENST00000531904.6:c.3400C>T
|
ENSP00000432391.2:p.Arg1134Ter
|
|
ENST00000531904.7:c.3400C>T
|
ENSP00000432391.3:p.Arg1134Ter
|
|
ENST00000533790.1:c.535C>T
|
ENSP00000436700.1:p.Arg179Ter
|
|
ENST00000533790.2:c.553C>T
|
ENSP00000436700.2:p.Arg185Ter
|
|
ENST00000533790.3:c.784C>T
|
ENSP00000436700.3:p.Arg262Ter
|
|
ENST00000534358.5:c.3301C>T
|
ENSP00000436786.1:p.Arg1101Ter
|
|
ENST00000648261.1:c.2071C>T
|
ENSP00000498126.1:p.Arg691Ter
|
|
ENST00000649690.2:c.1108C>T
|
ENSP00000497372.2:p.Arg370Ter
|
|
ENST00000649699.1:c.3301C>T
|
ENSP00000496927.1:p.Arg1101Ter
|
|
ENST00000685719.1:c.282C>T
|
|
|
ENST00000691053.1:c.3301C>T
|
ENSP00000509168.1:p.Arg1101Ter
|
|
ENST00000710560.1:c.3400C>T
|
ENSP00000518343.1:p.Arg1134Ter
|
|
XM_006718839.2:c.784C>T
|
XP_006718902.2:p.Arg262Ter
|
|
XM_006718839.3:c.784C>T
|
XP_006718902.2:p.Arg262Ter
|
|
XM_011542829.1:c.3400C>T
|
XP_011541131.1:p.Arg1134Ter
|
|
XM_011542829.2:c.3400C>T
|
XP_011541131.1:p.Arg1134Ter
|
|
XM_011542830.1:c.3400C>T
|
XP_011541132.1:p.Arg1134Ter
|
|
XM_011542830.2:c.3400C>T
|
XP_011541132.1:p.Arg1134Ter
|
|
XM_011542831.1:c.3400C>T
|
XP_011541133.1:p.Arg1134Ter
|
|
XM_011542831.2:c.3400C>T
|
XP_011541133.1:p.Arg1134Ter
|
|
XM_011542832.1:c.1207C>T
|
XP_011541134.1:p.Arg403Ter
|
|
XM_011542833.1:c.883C>T
|
XP_011541135.1:p.Arg295Ter
|
|
XM_011542833.2:c.883C>T
|
XP_011541135.1:p.Arg295Ter
|
