|
NM_005957.5:c.1603C>T
MANE Select
|
NP_005948.3:p.Arg535Trp
|
|
ENST00000376590.9:c.1603C>T
MANE Select
|
ENSP00000365775.3:p.Arg535Trp
|
|
NM_001330358.1:c.1726C>T
|
NP_001317287.1:p.Arg576Trp
|
|
NM_001330358.2:c.1726C>T
|
NP_001317287.1:p.Arg576Trp
|
|
NM_005957.4:c.1603C>T , LRG_726t1:c.1603C>T
|
NP_005948.3:p.Arg535Trp
|
|
ENST00000376583.7:c.1726C>T
|
ENSP00000365767.3:p.Arg576Trp
|
|
ENST00000376585.5:c.1726C>T
|
ENSP00000365770.1:p.Arg576Trp
|
|
ENST00000376585.6:c.1726C>T
|
ENSP00000365770.1:p.Arg576Trp
|
|
ENST00000376590.7:c.1603C>T
|
ENSP00000365775.3:p.Arg535Trp
|
|
ENST00000376592.5:c.1603C>T
|
ENSP00000365777.1:p.Arg535Trp
|
|
ENST00000376592.6:c.1603C>T
|
ENSP00000365777.1:p.Arg535Trp
|
|
ENST00000423400.7:c.1723C>T
|
ENSP00000398908.3:p.Arg575Trp
|
|
ENST00000641407.1:c.1603C>T
|
ENSP00000493098.1:p.Arg535Trp
|
|
ENST00000641446.1:c.1603C>T
|
ENSP00000493262.1:p.Arg535Trp
|
|
ENST00000641747.1:c.*1115C>T
|
ENSP00000493116.1:n.*1115C>T
|
|
ENST00000641759.1:n.1972C>T
|
|
|
ENST00000641805.1:n.2120C>T
|
|
|
ENST00000641820.1:c.868C>T
|
ENSP00000492937.1:p.Arg290Trp
|
|
XM_005263458.2:c.1726C>T
|
XP_005263515.1:p.Arg576Trp
|
|
XM_005263460.3:c.1603C>T
|
XP_005263517.1:p.Arg535Trp
|
|
XM_005263460.5:c.1603C>T
|
XP_005263517.1:p.Arg535Trp
|
|
XM_005263461.3:c.1603C>T
|
XP_005263518.1:p.Arg535Trp
|
|
XM_005263462.3:c.1603C>T
|
XP_005263519.1:p.Arg535Trp
|
|
XM_005263462.4:c.1603C>T
|
XP_005263519.1:p.Arg535Trp
|
|
XM_005263463.2:c.1357C>T
|
XP_005263520.1:p.Arg453Trp
|
|
XM_005263463.4:c.1357C>T
|
XP_005263520.1:p.Arg453Trp
|
|
XM_011541495.1:c.1723C>T
|
XP_011539797.1:p.Arg575Trp
|
|
XM_011541495.3:c.1723C>T
|
XP_011539797.1:p.Arg575Trp
|
|
XM_011541496.1:c.1726C>T
|
XP_011539798.1:p.Arg576Trp
|
|
XM_011541496.3:c.1726C>T
|
XP_011539798.1:p.Arg576Trp
|
|
XM_017001328.2:c.1726C>T
|
XP_016856817.1:p.Arg576Trp
|
|
XM_024447198.1:c.1357C>T
|
XP_024302966.1:p.Arg453Trp
|
|
XR_002956640.1:n.2704C>T
|
|
