ENST00000356392.9:c.1177A=
MANE Select
|
ENSP00000348757.3:p.Ser393=
|
|
ENST00000356392.8:c.1177A=
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ENSP00000348757.3:p.Ser393=
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|
ENST00000586836.5:c.604A=
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ENSP00000467429.1:p.Ser202=
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|
ENST00000591179.5:c.997A=
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ENSP00000466800.1:p.Ser333=
|
|
ENST00000591345.5:c.*1096A=
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ENSP00000467313.1:n.*1096A=
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|
NM_001302453.1:c.1015A=
|
NP_001289382.1:p.Ser339=
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|
NM_001302454.1:c.997A=
|
NP_001289383.1:p.Ser333=
|
|
NM_145045.4:c.1177A=
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NP_659482.3:p.Ser393=
|
|
XM_017026241.1:c.*71A=
|
XP_016881730.1:n.*71A=
|
|
NM_145045.5:c.1177A=
MANE Select
|
NP_659482.3:p.Ser393=
|
|
NM_001302454.2:c.997A=
|
NP_001289383.1:p.Ser333=
|
|