ENST00000317096.9:c.250G>T
MANE Select
|
ENSP00000325421.5:p.Glu84Ter
|
|
ENST00000638817.1:c.250G>T
|
ENSP00000492596.1:p.Glu84Ter
|
|
ENST00000639100.1:c.-444G>T
|
ENSP00000491186.1:n.-444G>T
|
|
ENST00000639401.1:c.250G>T
|
ENSP00000491227.1:p.Glu84Ter
|
|
ENST00000639900.1:c.250G>T
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ENSP00000491109.1:p.Glu84Ter
|
|
ENST00000311101.9:c.250G>T
|
ENSP00000310676.5:p.Glu84Ter
|
|
ENST00000317096.8:c.250G>T
|
ENSP00000325421.4:p.Glu84Ter
|
|
ENST00000421484.5:c.250G>T
|
ENSP00000404421.1:p.Glu84Ter
|
|
ENST00000435888.5:c.250G>T
|
ENSP00000402137.1:p.Glu84Ter
|
|
ENST00000449306.1:c.131G>T
|
|
|
ENST00000469056.1:n.172G>T
|
|
|
NM_001037639.1:c.250G>T
|
NP_001032728.1:p.Glu84Ter
|
|
NM_018622.5:c.250G>T
|
NP_061092.3:p.Glu84Ter
|
|
XM_005247582.3:c.250G>T
|
XP_005247639.1:p.Glu84Ter
|
|
XM_005247584.3:c.250G>T
|
XP_005247641.1:p.Glu84Ter
|
|
XM_005247587.1:c.-380G>T
|
XP_005247644.1:n.-380G>T
|
|
NM_001037639.2:c.250G>T
|
NP_001032728.1:p.Glu84Ter
|
|
NM_001324436.1:c.250G>T
|
NP_001311365.1:p.Glu84Ter
|
|
NM_001324437.1:c.250G>T
|
NP_001311366.1:p.Glu84Ter
|
|
NM_001324438.1:c.250G>T
|
NP_001311367.1:p.Glu84Ter
|
|
NM_018622.6:c.250G>T
|
NP_061092.3:p.Glu84Ter
|
|
NR_136893.1:n.312G>T
|
|
|
XM_005247582.5:c.250G>T
|
XP_005247639.1:p.Glu84Ter
|
|
XM_017006800.2:c.250G>T
|
XP_016862289.1:p.Glu84Ter
|
|
XM_017006801.1:c.250G>T
|
XP_016862290.1:p.Glu84Ter
|
|
XM_017006802.1:c.250G>T
|
XP_016862291.1:p.Glu84Ter
|
|
XM_017006803.1:c.-380G>T
|
XP_016862292.1:n.-380G>T
|
|
XM_024453628.1:c.-324G>T
|
XP_024309396.1:n.-324G>T
|
|
XM_024453629.1:c.-380G>T
|
XP_024309397.1:n.-380G>T
|
|
XM_024453630.1:c.-444G>T
|
XP_024309398.1:n.-444G>T
|
|
XM_024453631.1:c.-500G>T
|
XP_024309399.1:n.-500G>T
|
|
XM_024453632.1:c.-500G>T
|
XP_024309400.1:n.-500G>T
|
|
XM_024453633.1:c.-444G>T
|
XP_024309401.1:n.-444G>T
|
|
NM_001037639.3:c.250G>T
|
NP_001032728.1:p.Glu84Ter
|
|
NM_001324436.2:c.250G>T
|
NP_001311365.1:p.Glu84Ter
|
|
NM_001324437.2:c.250G>T
|
NP_001311366.1:p.Glu84Ter
|
|
NM_001324438.2:c.250G>T
|
NP_001311367.1:p.Glu84Ter
|
|
NM_018622.7:c.250G>T
MANE Select
|
NP_061092.3:p.Glu84Ter
|
|
NR_136893.2:n.284G>T
|
|
|