ENST00000373344.11:c.7274A>T
MANE Select
|
ENSP00000362441.4:p.Gln2425Leu
|
|
ENST00000675732.1:c.2372A>T
|
ENSP00000502598.1:p.Gln791Leu
|
|
ENST00000373344.9:c.7274A>T
|
ENSP00000362441.4:p.Gln2425Leu
|
|
ENST00000395603.7:c.7160A>T
|
ENSP00000378967.3:p.Gln2387Leu
|
|
ENST00000480283.5:c.*6902A>T
|
ENSP00000480196.1:n.*6902A>T
|
|
ENST00000623706.3:n.5594A>T
|
|
|
ENST00000624766.1:n.505A>T
|
|
|
NM_000489.4:c.7274A>T
|
NP_000480.3:p.Gln2425Leu
|
|
NM_138270.3:c.7160A>T
|
NP_612114.2:p.Gln2387Leu
|
|
XM_005262153.3:c.7271A>T
|
XP_005262210.2:p.Gln2424Leu
|
|
XM_005262154.3:c.7187A>T
|
XP_005262211.2:p.Gln2396Leu
|
|
XM_005262155.3:c.7157A>T
|
XP_005262212.2:p.Gln2386Leu
|
|
XM_005262156.3:c.7109A>T
|
XP_005262213.2:p.Gln2370Leu
|
|
XM_005262157.3:c.7070A>T
|
XP_005262214.2:p.Gln2357Leu
|
|
XM_006724666.2:c.7157A>T
|
XP_006724729.1:p.Gln2386Leu
|
|
XM_006724667.2:c.6995A>T
|
XP_006724730.1:p.Gln2332Leu
|
|
XR_938400.1:n.8866A>T
|
|
|
NM_000489.5:c.7274A>T
|
NP_000480.3:p.Gln2425Leu
|
|
XM_005262153.5:c.7271A>T
|
XP_005262210.2:p.Gln2424Leu
|
|
XM_005262154.5:c.7187A>T
|
XP_005262211.2:p.Gln2396Leu
|
|
XM_005262155.4:c.7157A>T
|
XP_005262212.2:p.Gln2386Leu
|
|
XM_005262156.4:c.7109A>T
|
XP_005262213.2:p.Gln2370Leu
|
|
XM_005262157.5:c.7070A>T
|
XP_005262214.2:p.Gln2357Leu
|
|
XM_006724666.4:c.7157A>T
|
XP_006724729.1:p.Gln2386Leu
|
|
XM_006724667.3:c.6995A>T
|
XP_006724730.1:p.Gln2332Leu
|
|
XM_017029601.2:c.7184A>T
|
XP_016885090.1:p.Gln2395Leu
|
|
XM_017029602.1:c.7154A>T
|
XP_016885091.1:p.Gln2385Leu
|
|
XM_017029603.1:c.7106A>T
|
XP_016885092.1:p.Gln2369Leu
|
|
XM_017029604.2:c.7073A>T
|
XP_016885093.1:p.Gln2358Leu
|
|
XM_017029605.1:c.7070A>T
|
XP_016885094.1:p.Gln2357Leu
|
|
XM_017029606.2:c.7043A>T
|
XP_016885095.1:p.Gln2348Leu
|
|
XM_017029607.2:c.7040A>T
|
XP_016885096.1:p.Gln2347Leu
|
|
XM_017029608.2:c.6992A>T
|
XP_016885097.1:p.Gln2331Leu
|
|
XM_017029609.1:c.6956A>T
|
XP_016885098.1:p.Gln2319Leu
|
|
XM_017029610.1:c.6953A>T
|
XP_016885099.1:p.Gln2318Leu
|
|
XM_017029611.1:c.6908A>T
|
XP_016885100.1:p.Gln2303Leu
|
|
XR_001755700.2:n.7573A>T
|
|
|
NM_138270.4:c.7160A>T
|
NP_612114.2:p.Gln2387Leu
|
|
NM_000489.6:c.7274A>T
MANE Select
|
NP_000480.3:p.Gln2425Leu
|
|
NM_138270.5:c.7160A>T
|
NP_612114.2:p.Gln2387Leu
|
|