ENST00000278853.10:c.1661G>A
MANE Select
|
ENSP00000278853.5:p.Arg554Gln
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|
ENST00000278853.9:c.1661G>A
|
ENSP00000278853.5:p.Arg554Gln
|
|
ENST00000537203.5:n.1280G>A
|
|
|
ENST00000620319.1:c.782G>A
|
ENSP00000480463.1:p.Arg261Gln
|
|
NM_207341.3:c.1661G>A
|
NP_997224.2:p.Arg554Gln
|
|
XM_011544852.1:c.782G>A
|
XP_011543154.1:p.Arg261Gln
|
|
XM_011544853.1:c.782G>A
|
XP_011543155.1:p.Arg261Gln
|
|
XM_011544852.2:c.782G>A
|
XP_011543154.1:p.Arg261Gln
|
|
XM_011544853.2:c.782G>A
|
XP_011543155.1:p.Arg261Gln
|
|
NM_001391943.1:c.782G>A
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NP_001378872.1:p.Arg261Gln
|
|
NM_001391944.1:c.467G>A
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NP_001378873.1:p.Arg156Gln
|
|
NM_207341.4:c.1661G>A
MANE Select
|
NP_997224.2:p.Arg554Gln
|
|