ENST00000456935.7:c.2671G>C
MANE Select
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ENSP00000395473.2:p.Gly891Arg
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ENST00000221363.8:c.2668G>C
|
ENSP00000221363.4:p.Gly890Arg
|
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ENST00000456935.6:c.2671G>C
|
ENSP00000395473.2:p.Gly891Arg
|
|
ENST00000466794.5:n.3261G>C
|
|
|
ENST00000493218.5:n.82G>C
|
|
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ENST00000597692.1:c.230G>C
|
|
|
NM_000528.3:c.2671G>C
|
NP_000519.2:p.Gly891Arg
|
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NM_001173498.1:c.2668G>C
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NP_001166969.1:p.Gly890Arg
|
|
XM_005259913.1:c.2674G>C
|
XP_005259970.1:p.Gly892Arg
|
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XM_011528017.1:c.1570G>C
|
XP_011526319.1:p.Gly524Arg
|
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XM_005259913.2:c.2674G>C
|
XP_005259970.1:p.Gly892Arg
|
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XM_024451518.1:c.1570G>C
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XP_024307286.1:p.Gly524Arg
|
|
NM_000528.4:c.2671G>C
MANE Select
|
NP_000519.2:p.Gly891Arg
|
|
NM_001173498.2:c.2668G>C
|
NP_001166969.1:p.Gly890Arg
|
|