ENST00000265104.5:c.8001G>C
MANE Select
|
ENSP00000265104.4:p.Trp2667Cys
|
|
ENST00000681290.1:c.7956G>C
|
ENSP00000505288.1:p.Trp2652Cys
|
|
ENST00000265104.4:c.8001G>C
|
ENSP00000265104.4:p.Trp2667Cys
|
|
NM_001369.2:c.8001G>C
|
NP_001360.1:p.Trp2667Cys
|
|
XM_005248262.2:c.7956G>C
|
XP_005248319.1:p.Trp2652Cys
|
|
XM_011513990.1:c.8001G>C
|
XP_011512292.1:p.Trp2667Cys
|
|
XR_925598.1:n.8208G>C
|
|
|
XM_005248262.3:c.8109G>C
|
XP_005248319.2:p.Trp2703Cys
|
|
XM_017009177.1:c.8109G>C
|
XP_016864666.1:p.Trp2703Cys
|
|
XM_017009178.1:c.7014G>C
|
XP_016864667.1:p.Trp2338Cys
|
|
XM_017009179.2:c.7014G>C
|
XP_016864668.1:p.Trp2338Cys
|
|
XM_017009180.1:c.8109G>C
|
XP_016864669.1:p.Trp2703Cys
|
|
XM_017009181.1:c.8109G>C
|
XP_016864670.1:p.Trp2703Cys
|
|
XM_017009182.1:c.8109G>C
|
XP_016864671.1:p.Trp2703Cys
|
|
XM_017009183.1:c.8109G>C
|
XP_016864672.1:p.Trp2703Cys
|
|
XM_017009184.1:c.8109G>C
|
XP_016864673.1:p.Trp2703Cys
|
|
XM_017009185.1:c.3198G>C
|
XP_016864674.1:p.Trp1066Cys
|
|
XM_017009186.1:c.2751G>C
|
XP_016864675.1:p.Trp917Cys
|
|
XM_017009188.1:c.2088G>C
|
XP_016864677.1:p.Trp696Cys
|
|
XM_024454388.1:c.7014G>C
|
XP_024310156.1:p.Trp2338Cys
|
|
XM_024454389.1:c.6603G>C
|
XP_024310157.1:p.Trp2201Cys
|
|
XR_001742034.1:n.8126G>C
|
|
|
XR_001742035.1:n.8126G>C
|
|
|
NM_001369.3:c.8001G>C
MANE Select
|
NP_001360.1:p.Trp2667Cys
|
|