ENST00000274376.11:c.2963G>T
(RASA1)
MANE Select
|
ENSP00000274376.6:p.Arg988Ile
|
|
ENST00000645953.1:c.*90+3340C>A
(CCNH)
|
ENSP00000494460.1:n.*90+3340C>A
|
|
ENST00000646883.1:c.254+3340C>A
(CCNH)
|
|
|
ENST00000274376.10:c.2963G>T
(RASA1)
|
ENSP00000274376.6:p.Arg988Ile
|
|
ENST00000456692.6:c.2432G>T
(RASA1)
|
ENSP00000411221.2:p.Arg811Ile
|
|
ENST00000506290.1:c.2465G>T
(RASA1)
|
ENSP00000420905.1:p.Arg822Ile
|
|
ENST00000512763.5:c.2462G>T
(RASA1)
|
ENSP00000422008.1:p.Arg821Ile
|
|
ENST00000515800.6:c.*1578G>T
(RASA1)
|
ENSP00000423395.2:n.*1578G>T
|
|
NM_002890.2:c.2963G>T
(RASA1)
|
NP_002881.1:p.Arg988Ile
|
|
NM_022650.2:c.2432G>T
(RASA1)
|
NP_072179.1:p.Arg811Ile
|
|
XM_011543525.1:c.2876G>T
(RASA1)
|
XP_011541827.1:p.Arg959Ile
|
|
NM_001364075.1:c.933+5614C>A
(CCNH)
|
NP_001351004.1:n.933+5614C>A
|
|
NR_157068.1:n.1447+3340C>A
(CCNH)
|
|
|
NR_157069.1:n.1040+3340C>A
(CCNH)
|
|
|
NR_157070.1:n.1204+3340C>A
(CCNH)
|
|
|
XM_011543525.2:c.2876G>T
(RASA1)
|
XP_011541827.1:p.Arg959Ile
|
|
NM_001364075.2:c.933+5614C>A
(CCNH)
|
NP_001351004.1:n.933+5614C>A
|
|
NM_002890.3:c.2963G>T
(RASA1)
MANE Select
|
NP_002881.1:p.Arg988Ile
|
|
NR_157068.2:n.1447+3340C>A
(CCNH)
|
|
|
NR_157069.2:n.1040+3340C>A
(CCNH)
|
|
|
NR_157070.2:n.1204+3340C>A
(CCNH)
|
|
|
NM_022650.3:c.2432G>T
(RASA1)
|
NP_072179.1:p.Arg811Ile
|
|