ENST00000274376.11:c.1935T>G
(RASA1)
MANE Select
|
ENSP00000274376.6:p.Asp645Glu
|
|
ENST00000645953.1:c.*90+17930A>C
(CCNH)
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ENSP00000494460.1:n.*90+17930A>C
|
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ENST00000274376.10:c.1935T>G
(RASA1)
|
ENSP00000274376.6:p.Asp645Glu
|
|
ENST00000456692.6:c.1404T>G
(RASA1)
|
ENSP00000411221.2:p.Asp468Glu
|
|
ENST00000506290.1:c.1437T>G
(RASA1)
|
ENSP00000420905.1:p.Asp479Glu
|
|
ENST00000512763.5:c.1434T>G
(RASA1)
|
ENSP00000422008.1:p.Asp478Glu
|
|
ENST00000515800.6:c.*460T>G
(RASA1)
|
ENSP00000423395.2:n.*460T>G
|
|
NM_002890.2:c.1935T>G
(RASA1)
|
NP_002881.1:p.Asp645Glu
|
|
NM_022650.2:c.1404T>G
(RASA1)
|
NP_072179.1:p.Asp468Glu
|
|
XM_011543525.1:c.1935T>G
(RASA1)
|
XP_011541827.1:p.Asp645Glu
|
|
XM_011543526.1:c.1935T>G
(RASA1)
|
XP_011541828.1:p.Asp645Glu
|
|
XR_948544.1:n.742+805A>C
|
|
|
NM_001364075.1:c.933+20204A>C
(CCNH)
|
NP_001351004.1:n.933+20204A>C
|
|
NR_157068.1:n.1447+17930A>C
(CCNH)
|
|
|
NR_157069.1:n.1040+17930A>C
(CCNH)
|
|
|
NR_157070.1:n.1204+17930A>C
(CCNH)
|
|
|
XM_011543525.2:c.1935T>G
(RASA1)
|
XP_011541827.1:p.Asp645Glu
|
|
NM_001364075.2:c.933+20204A>C
(CCNH)
|
NP_001351004.1:n.933+20204A>C
|
|
NM_002890.3:c.1935T>G
(RASA1)
MANE Select
|
NP_002881.1:p.Asp645Glu
|
|
NR_157068.2:n.1447+17930A>C
(CCNH)
|
|
|
NR_157069.2:n.1040+17930A>C
(CCNH)
|
|
|
NR_157070.2:n.1204+17930A>C
(CCNH)
|
|
|
NM_022650.3:c.1404T>G
(RASA1)
|
NP_072179.1:p.Asp468Glu
|
|