ENST00000274376.11:c.2938C>T
(RASA1)
MANE Select
|
ENSP00000274376.6:p.Leu980Phe
|
|
ENST00000645953.1:c.*90+3365G>A
(CCNH)
|
ENSP00000494460.1:n.*90+3365G>A
|
|
ENST00000646883.1:c.254+3365G>A
(CCNH)
|
|
|
ENST00000274376.10:c.2938C>T
(RASA1)
|
ENSP00000274376.6:p.Leu980Phe
|
|
ENST00000456692.6:c.2407C>T
(RASA1)
|
ENSP00000411221.2:p.Leu803Phe
|
|
ENST00000506290.1:c.2440C>T
(RASA1)
|
ENSP00000420905.1:p.Leu814Phe
|
|
ENST00000512763.5:c.2437C>T
(RASA1)
|
ENSP00000422008.1:p.Leu813Phe
|
|
ENST00000515800.6:c.*1553C>T
(RASA1)
|
ENSP00000423395.2:n.*1553C>T
|
|
NM_002890.2:c.2938C>T
(RASA1)
|
NP_002881.1:p.Leu980Phe
|
|
NM_022650.2:c.2407C>T
(RASA1)
|
NP_072179.1:p.Leu803Phe
|
|
XM_011543525.1:c.2851C>T
(RASA1)
|
XP_011541827.1:p.Leu951Phe
|
|
NM_001364075.1:c.933+5639G>A
(CCNH)
|
NP_001351004.1:n.933+5639G>A
|
|
NR_157068.1:n.1447+3365G>A
(CCNH)
|
|
|
NR_157069.1:n.1040+3365G>A
(CCNH)
|
|
|
NR_157070.1:n.1204+3365G>A
(CCNH)
|
|
|
XM_011543525.2:c.2851C>T
(RASA1)
|
XP_011541827.1:p.Leu951Phe
|
|
NM_001364075.2:c.933+5639G>A
(CCNH)
|
NP_001351004.1:n.933+5639G>A
|
|
NM_002890.3:c.2938C>T
(RASA1)
MANE Select
|
NP_002881.1:p.Leu980Phe
|
|
NR_157068.2:n.1447+3365G>A
(CCNH)
|
|
|
NR_157069.2:n.1040+3365G>A
(CCNH)
|
|
|
NR_157070.2:n.1204+3365G>A
(CCNH)
|
|
|
NM_022650.3:c.2407C>T
(RASA1)
|
NP_072179.1:p.Leu803Phe
|
|