ENST00000339818.9:c.281T>G
MANE Select
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ENSP00000344566.4:p.Leu94Arg
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ENST00000325223.7:c.281T>G
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ENSP00000317302.7:p.Leu94Arg
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ENST00000339818.8:c.281T>G
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ENSP00000344566.4:p.Leu94Arg
|
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ENST00000397956.7:c.281T>G
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ENSP00000381047.3:p.Leu94Arg
|
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ENST00000462742.1:n.2452T>G
|
|
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ENST00000478674.1:n.340T>G
|
|
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ENST00000496321.5:n.397T>G
|
|
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NM_001271440.1:c.281T>G
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NP_001258369.1:p.Leu94Arg
|
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NM_001271441.1:c.281T>G
|
NP_001258370.1:p.Leu94Arg
|
|
NM_001271442.1:c.158T>G
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NP_001258371.1:p.Leu53Arg
|
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NM_004928.2:c.281T>G
|
NP_004919.1:p.Leu94Arg
|
|
XM_006724051.2:c.356T>G
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XP_006724114.1:p.Leu119Arg
|
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XM_006724052.2:c.356T>G
|
XP_006724115.1:p.Leu119Arg
|
|
XM_006724053.2:c.-44T>G
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XP_006724116.1:n.-44T>G
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XR_937571.1:n.484T>G
|
|
|
XM_006724051.3:c.356T>G
|
XP_006724114.1:p.Leu119Arg
|
|
XM_006724053.3:c.-44T>G
|
XP_006724116.1:n.-44T>G
|
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XM_017028470.1:c.485T>G
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XP_016883959.1:p.Leu162Arg
|
|
XM_017028471.1:c.230T>G
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XP_016883960.1:p.Leu77Arg
|
|
XM_017028472.1:c.-44T>G
|
XP_016883961.1:n.-44T>G
|
|
XR_937571.2:n.491T>G
|
|
|
NM_004928.3:c.281T>G
MANE Select
|
NP_004919.1:p.Leu94Arg
|
|
NM_001271440.2:c.281T>G
|
NP_001258369.1:p.Leu94Arg
|
|
NM_001271441.2:c.281T>G
|
NP_001258370.1:p.Leu94Arg
|
|