ENST00000376486.3:c.18A>C
|
ENSP00000365669.3:p.Arg6Ser
|
|
ENST00000376585.6:c.141A>C
|
ENSP00000365770.1:p.Arg47Ser
|
|
ENST00000376590.9:c.18A>C
MANE Select
|
ENSP00000365775.3:p.Arg6Ser
|
|
ENST00000376592.6:c.18A>C
|
ENSP00000365777.1:p.Arg6Ser
|
|
ENST00000423400.7:c.138A>C
|
ENSP00000398908.3:p.Arg46Ser
|
|
ENST00000431243.6:n.799A>C
|
|
|
ENST00000641407.1:c.18A>C
|
ENSP00000493098.1:p.Arg6Ser
|
|
ENST00000641437.1:n.150A>C
|
|
|
ENST00000641446.1:c.18A>C
|
ENSP00000493262.1:p.Arg6Ser
|
|
ENST00000641721.1:n.75A>C
|
|
|
ENST00000641747.1:c.18A>C
|
ENSP00000493116.1:p.Arg6Ser
|
|
ENST00000641759.1:n.153A>C
|
|
|
ENST00000641805.1:n.301A>C
|
|
|
ENST00000641909.1:n.428A>C
|
|
|
ENST00000642002.1:n.247A>C
|
|
|
ENST00000376486.2:c.18A>C
|
ENSP00000365669.2:p.Arg6Ser
|
|
ENST00000376583.7:c.141A>C
|
ENSP00000365767.3:p.Arg47Ser
|
|
ENST00000376585.5:c.141A>C
|
ENSP00000365770.1:p.Arg47Ser
|
|
ENST00000376590.7:c.18A>C
|
ENSP00000365775.3:p.Arg6Ser
|
|
ENST00000376592.5:c.18A>C
|
ENSP00000365777.1:p.Arg6Ser
|
|
ENST00000413656.5:c.18A>C
|
ENSP00000408307.1:p.Arg6Ser
|
|
ENST00000418034.1:c.18A>C
|
ENSP00000405082.1:p.Arg6Ser
|
|
ENST00000423400.5:c.87A>C
|
ENSP00000398908.1:p.Arg29Ser
|
|
ENST00000431243.5:c.18A>C
|
ENSP00000400460.1:p.Arg6Ser
|
|
NM_005957.4:c.18A>C , LRG_726t1:c.18A>C
|
NP_005948.3:p.Arg6Ser
|
|
XM_005263458.2:c.141A>C
|
XP_005263515.1:p.Arg47Ser
|
|
XM_005263460.3:c.18A>C
|
XP_005263517.1:p.Arg6Ser
|
|
XM_005263461.3:c.18A>C
|
XP_005263518.1:p.Arg6Ser
|
|
XM_005263462.3:c.18A>C
|
XP_005263519.1:p.Arg6Ser
|
|
XM_005263463.2:c.-246A>C
|
XP_005263520.1:n.-246A>C
|
|
XM_011541495.1:c.138A>C
|
XP_011539797.1:p.Arg46Ser
|
|
XM_011541496.1:c.141A>C
|
XP_011539798.1:p.Arg47Ser
|
|
NM_001330358.1:c.141A>C
|
NP_001317287.1:p.Arg47Ser
|
|
XM_005263460.5:c.18A>C
|
XP_005263517.1:p.Arg6Ser
|
|
XM_005263462.4:c.18A>C
|
XP_005263519.1:p.Arg6Ser
|
|
XM_005263463.4:c.-246A>C
|
XP_005263520.1:n.-246A>C
|
|
XM_011541495.3:c.138A>C
|
XP_011539797.1:p.Arg46Ser
|
|
XM_011541496.3:c.141A>C
|
XP_011539798.1:p.Arg47Ser
|
|
XM_017001328.2:c.141A>C
|
XP_016856817.1:p.Arg47Ser
|
|
XM_024447198.1:c.-246A>C
|
XP_024302966.1:n.-246A>C
|
|
XR_002956640.1:n.885A>C
|
|
|
NM_005957.5:c.18A>C
MANE Select
|
NP_005948.3:p.Arg6Ser
|
|
NM_001330358.2:c.141A>C
|
NP_001317287.1:p.Arg47Ser
|
|