ENST00000216714.8:c.693C>T
MANE Select
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ENSP00000216714.3:p.Gly231=
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ENST00000216714.7:c.693C>T
|
ENSP00000216714.3:p.Gly231=
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|
ENST00000398030.8:c.693C>T
|
ENSP00000381111.4:p.Gly231=
|
|
ENST00000553555.5:n.1113C>T
|
|
|
ENST00000553681.5:c.693C>T
|
ENSP00000451327.1:p.Gly231=
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|
ENST00000555414.5:c.693C>T
|
ENSP00000451979.1:p.Gly231=
|
|
ENST00000555839.5:c.606C>T
|
ENSP00000452460.1:p.Gly202=
|
|
ENST00000557054.1:c.*104C>T
|
ENSP00000452212.2:n.*104C>T
|
|
ENST00000557159.5:n.1309C>T
|
|
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ENST00000557365.1:n.773C>T
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|
|
NM_001244249.1:c.693C>T
|
NP_001231178.1:p.Gly231=
|
|
NM_001641.3:c.693C>T
|
NP_001632.2:p.Gly231=
|
|
NM_080648.2:c.693C>T
|
NP_542379.1:p.Gly231=
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|
NM_080649.2:c.693C>T
|
NP_542380.1:p.Gly231=
|
|
XM_005267581.3:c.693C>T
|
XP_005267638.1:p.Gly231=
|
|
XM_005267582.3:c.642C>T
|
XP_005267639.1:p.Gly214=
|
|
NM_001641.4:c.693C>T
MANE Select
|
NP_001632.2:p.Gly231=
|
|
NM_001244249.2:c.693C>T
|
NP_001231178.1:p.Gly231=
|
|
NM_080648.3:c.693C>T
|
NP_542379.1:p.Gly231=
|
|
NM_080649.3:c.693C>T
|
NP_542380.1:p.Gly231=
|
|