ENST00000261647.10:c.45G>A
MANE Select
|
ENSP00000261647.5:p.Arg15=
|
|
ENST00000261647.9:c.45G>A
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ENSP00000261647.5:p.Arg15=
|
|
ENST00000466729.5:c.110G>A
|
|
|
ENST00000470399.1:c.60G>A
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ENSP00000465082.1:p.Arg20=
|
|
ENST00000475723.5:c.92G>A
|
|
|
ENST00000497842.6:n.70G>A
|
|
|
ENST00000583704.1:n.70G>A
|
|
|
NM_001271420.1:c.-414G>A
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NP_001258349.1:n.-414G>A
|
|
NM_017775.3:c.45G>A
|
NP_060245.3:p.Arg15=
|
|
XM_011523950.1:c.45G>A
|
XP_011522252.1:p.Arg15=
|
|
XM_017024801.2:c.45G>A
|
XP_016880290.2:p.Arg15=
|
|
XM_017024802.2:c.45G>A
|
XP_016880291.2:p.Arg15=
|
|
XM_024450814.1:c.45G>A
|
XP_024306582.1:p.Arg15=
|
|
NM_017775.4:c.45G>A
MANE Select
|
NP_060245.3:p.Arg15=
|
|
NM_001271420.2:c.-414G>A
|
NP_001258349.1:n.-414G>A
|
|