ENST00000298139.7:c.4255A>G
MANE Select
|
ENSP00000298139.5:p.Lys1419Glu
|
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ENST00000650667.1:c.*3869A>G
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ENSP00000498593.1:n.*3869A>G
|
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ENST00000651946.1:n.479A>G
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|
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ENST00000298139.5:c.4255A>G
|
ENSP00000298139.5:p.Lys1419Glu
|
|
ENST00000521620.5:n.2888A>G
|
|
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NM_000553.4:c.4255A>G , LRG_524t1:c.4255A>G
|
NP_000544.2:p.Lys1419Glu
|
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XM_011544639.1:c.4174A>G
|
XP_011542941.1:p.Lys1392Glu
|
|
XM_011544640.1:c.2656A>G
|
XP_011542942.1:p.Lys886Glu
|
|
XR_949643.1:n.88-1740T>C
|
|
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XR_949644.1:n.88-1740T>C
|
|
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XR_949645.1:n.88-1740T>C
|
|
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XR_949646.1:n.88-1740T>C
|
|
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XR_949647.1:n.701-1740T>C
|
|
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XR_949648.1:n.603-1740T>C
|
|
|
NM_000553.5:c.4255A>G
|
NP_000544.2:p.Lys1419Glu
|
|
XM_011544639.3:c.4174A>G
|
XP_011542941.1:p.Lys1392Glu
|
|
XM_024447265.1:c.4045A>G
|
XP_024303033.1:p.Lys1349Glu
|
|
NM_000553.6:c.4255A>G
MANE Select
|
NP_000544.2:p.Lys1419Glu
|
|