ENST00000356392.9:c.1143G>T
MANE Select
|
ENSP00000348757.3:p.Gln381His
|
|
ENST00000356392.8:c.1143G>T
|
ENSP00000348757.3:p.Gln381His
|
|
ENST00000586836.5:c.570G>T
|
ENSP00000467429.1:p.Gln190His
|
|
ENST00000591179.5:c.963G>T
|
ENSP00000466800.1:p.Gln321His
|
|
ENST00000591345.5:c.*1062G>T
|
ENSP00000467313.1:n.*1062G>T
|
|
NM_001302453.1:c.981G>T
|
NP_001289382.1:p.Gln327His
|
|
NM_001302454.1:c.963G>T
|
NP_001289383.1:p.Gln321His
|
|
NM_145045.4:c.1143G>T
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NP_659482.3:p.Gln381His
|
|
XM_017026241.1:c.*37G>T
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XP_016881730.1:n.*37G>T
|
|
NM_145045.5:c.1143G>T
MANE Select
|
NP_659482.3:p.Gln381His
|
|
NM_001302454.2:c.963G>T
|
NP_001289383.1:p.Gln321His
|
|