ENST00000440970.6:c.*861A=
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ENSP00000407914.2:n.*861A=
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|
ENST00000685868.1:c.*861A=
|
ENSP00000509873.1:n.*861A=
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|
ENST00000251020.9:c.*861A=
MANE Select
|
ENSP00000251020.4:n.*861A=
|
|
ENST00000251020.8:c.*861A=
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ENSP00000251020.4:n.*861A=
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|
ENST00000440970.5:c.*861A=
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ENSP00000407914.1:n.*861A=
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|
NM_001127892.1:c.*861A=
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NP_001121364.1:n.*861A=
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|
NM_002968.2:c.*861A= , LRG_674t1:c.*861A=
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NP_002959.2:n.*861A=
|
|
XM_006721241.2:c.*861A=
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XP_006721304.1:n.*861A=
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|
XM_011523254.1:c.*861A=
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XP_011521556.1:n.*861A=
|
|
XM_011523255.1:c.*861A=
|
XP_011521557.1:n.*861A=
|
|
NM_002968.3:c.*861A=
MANE Select
|
NP_002959.2:n.*861A=
|
|
NM_001127892.2:c.*861A=
|
NP_001121364.1:n.*861A=
|
|