ENST00000274376.11:c.2926A>C
(RASA1)
MANE Select
|
ENSP00000274376.6:p.Asn976His
|
|
ENST00000645953.1:c.*90+3377T>G
(CCNH)
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ENSP00000494460.1:n.*90+3377T>G
|
|
ENST00000646883.1:c.254+3377T>G
(CCNH)
|
|
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ENST00000274376.10:c.2926A>C
(RASA1)
|
ENSP00000274376.6:p.Asn976His
|
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ENST00000456692.6:c.2395A>C
(RASA1)
|
ENSP00000411221.2:p.Asn799His
|
|
ENST00000506290.1:c.2428A>C
(RASA1)
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ENSP00000420905.1:p.Asn810His
|
|
ENST00000512763.5:c.2425A>C
(RASA1)
|
ENSP00000422008.1:p.Asn809His
|
|
ENST00000515800.6:c.*1541A>C
(RASA1)
|
ENSP00000423395.2:n.*1541A>C
|
|
NM_002890.2:c.2926A>C
(RASA1)
|
NP_002881.1:p.Asn976His
|
|
NM_022650.2:c.2395A>C
(RASA1)
|
NP_072179.1:p.Asn799His
|
|
XM_011543525.1:c.2839A>C
(RASA1)
|
XP_011541827.1:p.Asn947His
|
|
NM_001364075.1:c.933+5651T>G
(CCNH)
|
NP_001351004.1:n.933+5651T>G
|
|
NR_157068.1:n.1447+3377T>G
(CCNH)
|
|
|
NR_157069.1:n.1040+3377T>G
(CCNH)
|
|
|
NR_157070.1:n.1204+3377T>G
(CCNH)
|
|
|
XM_011543525.2:c.2839A>C
(RASA1)
|
XP_011541827.1:p.Asn947His
|
|
NM_001364075.2:c.933+5651T>G
(CCNH)
|
NP_001351004.1:n.933+5651T>G
|
|
NM_002890.3:c.2926A>C
(RASA1)
MANE Select
|
NP_002881.1:p.Asn976His
|
|
NR_157068.2:n.1447+3377T>G
(CCNH)
|
|
|
NR_157069.2:n.1040+3377T>G
(CCNH)
|
|
|
NR_157070.2:n.1204+3377T>G
(CCNH)
|
|
|
NM_022650.3:c.2395A>C
(RASA1)
|
NP_072179.1:p.Asn799His
|
|