ENST00000265104.5:c.1935G>C
MANE Select
|
ENSP00000265104.4:p.Gln645His
|
|
ENST00000681290.1:c.1890G>C
|
ENSP00000505288.1:p.Gln630His
|
|
ENST00000265104.4:c.1935G>C
|
ENSP00000265104.4:p.Gln645His
|
|
NM_001369.2:c.1935G>C
|
NP_001360.1:p.Gln645His
|
|
XM_005248262.2:c.1890G>C
|
XP_005248319.1:p.Gln630His
|
|
XM_011513990.1:c.1935G>C
|
XP_011512292.1:p.Gln645His
|
|
XR_925598.1:n.2142G>C
|
|
|
XM_005248262.3:c.2043G>C
|
XP_005248319.2:p.Gln681His
|
|
XM_017009177.1:c.2043G>C
|
XP_016864666.1:p.Gln681His
|
|
XM_017009178.1:c.948G>C
|
XP_016864667.1:p.Gln316His
|
|
XM_017009179.2:c.948G>C
|
XP_016864668.1:p.Gln316His
|
|
XM_017009180.1:c.2043G>C
|
XP_016864669.1:p.Gln681His
|
|
XM_017009181.1:c.2043G>C
|
XP_016864670.1:p.Gln681His
|
|
XM_017009182.1:c.2043G>C
|
XP_016864671.1:p.Gln681His
|
|
XM_017009183.1:c.2043G>C
|
XP_016864672.1:p.Gln681His
|
|
XM_017009184.1:c.2043G>C
|
XP_016864673.1:p.Gln681His
|
|
XM_017009187.1:c.2043G>C
|
XP_016864676.1:p.Gln681His
|
|
XM_024454388.1:c.948G>C
|
XP_024310156.1:p.Gln316His
|
|
XM_024454389.1:c.537G>C
|
XP_024310157.1:p.Gln179His
|
|
XR_001742034.1:n.2060G>C
|
|
|
XR_001742035.1:n.2060G>C
|
|
|
NM_001369.3:c.1935G>C
MANE Select
|
NP_001360.1:p.Gln645His
|
|