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NM_145045.5:c.787G>T
MANE Select
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NP_659482.3:p.Glu263Ter
|
|
ENST00000356392.9:c.787G>T
MANE Select
|
ENSP00000348757.3:p.Glu263Ter
|
|
NM_001302453.1:c.625G>T
|
NP_001289382.1:p.Glu209Ter
|
|
NM_001302454.1:c.607G>T
|
NP_001289383.1:p.Glu203Ter
|
|
NM_001302454.2:c.607G>T
|
NP_001289383.1:p.Glu203Ter
|
|
NM_145045.4:c.787G>T
|
NP_659482.3:p.Glu263Ter
|
|
ENST00000356392.8:c.787G>T
|
ENSP00000348757.3:p.Glu263Ter
|
|
ENST00000586836.5:c.214G>T
|
ENSP00000467429.1:p.Glu72Ter
|
|
ENST00000591179.5:c.607G>T
|
ENSP00000466800.1:p.Glu203Ter
|
|
ENST00000591345.5:c.*706G>T
|
ENSP00000467313.1:n.*706G>T
|
|
XM_017026241.1:c.787G>T
|
XP_016881730.1:p.Glu263Ter
|