ENST00000374448.9:c.2266T>C
MANE Select
|
ENSP00000363571.4:p.Tyr756His
|
|
ENST00000189978.10:c.2008T>C
|
ENSP00000189978.6:p.Tyr670His
|
|
ENST00000374440.7:c.2008T>C
|
ENSP00000363563.4:p.Tyr670His
|
|
ENST00000374448.8:c.2266T>C
|
ENSP00000363571.4:p.Tyr756His
|
|
ENST00000416899.7:c.2242T>C
|
ENSP00000393608.3:p.Tyr748His
|
|
NM_001166280.1:c.2008T>C
|
NP_001159752.1:p.Tyr670His
|
|
NM_001166281.1:c.1978T>C
|
NP_001159753.1:p.Tyr660His
|
|
NM_005592.3:c.2266T>C
|
NP_005583.1:p.Tyr756His
|
|
XM_005251994.2:c.2296T>C
|
XP_005252051.1:p.Tyr766His
|
|
XM_005251995.2:c.2272T>C
|
XP_005252052.1:p.Tyr758His
|
|
XM_005251996.2:c.2242T>C
|
XP_005252053.1:p.Tyr748His
|
|
XM_011518707.1:c.2326T>C
|
XP_011517009.1:p.Tyr776His
|
|
XM_011518708.1:c.1030T>C
|
XP_011517010.1:p.Tyr344His
|
|
XM_005251994.3:c.2296T>C
|
XP_005252051.1:p.Tyr766His
|
|
XM_005251995.3:c.2272T>C
|
XP_005252052.1:p.Tyr758His
|
|
XM_005251996.3:c.2242T>C
|
XP_005252053.1:p.Tyr748His
|
|
XM_011518708.2:c.1030T>C
|
XP_011517010.1:p.Tyr344His
|
|
XM_017014734.1:c.2032T>C
|
XP_016870223.1:p.Tyr678His
|
|
NM_001166280.2:c.2008T>C
|
NP_001159752.1:p.Tyr670His
|
|
NM_001166281.2:c.1978T>C
|
NP_001159753.1:p.Tyr660His
|
|
NM_001369398.1:c.1006T>C
|
NP_001356327.1:p.Tyr336His
|
|
NM_005592.4:c.2266T>C
MANE Select
|
NP_005583.1:p.Tyr756His
|
|