ENST00000274376.11:c.1325C>G
(RASA1)
MANE Select
|
ENSP00000274376.6:p.Pro442Arg
|
|
ENST00000645953.1:c.*91-34331G>C
(CCNH)
|
ENSP00000494460.1:n.*91-34331G>C
|
|
ENST00000274376.10:c.1325C>G
(RASA1)
|
ENSP00000274376.6:p.Pro442Arg
|
|
ENST00000456692.6:c.794C>G
(RASA1)
|
ENSP00000411221.2:p.Pro265Arg
|
|
ENST00000506290.1:c.827C>G
(RASA1)
|
ENSP00000420905.1:p.Pro276Arg
|
|
ENST00000509953.1:n.428C>G
(RASA1)
|
|
|
ENST00000512763.5:c.824C>G
(RASA1)
|
ENSP00000422008.1:p.Pro275Arg
|
|
ENST00000515800.6:c.1325C>G
(RASA1)
|
ENSP00000423395.2:p.Pro442Arg
|
|
NM_002890.2:c.1325C>G
(RASA1)
|
NP_002881.1:p.Pro442Arg
|
|
NM_022650.2:c.794C>G
(RASA1)
|
NP_072179.1:p.Pro265Arg
|
|
XM_011543525.1:c.1325C>G
(RASA1)
|
XP_011541827.1:p.Pro442Arg
|
|
XM_011543526.1:c.1325C>G
(RASA1)
|
XP_011541828.1:p.Pro442Arg
|
|
XM_011543527.1:c.1325C>G
(RASA1)
|
XP_011541829.1:p.Pro442Arg
|
|
NM_001364075.1:c.934-40433G>C
(CCNH)
|
NP_001351004.1:n.934-40433G>C
|
|
NR_157068.1:n.1447+39542G>C
(CCNH)
|
|
|
NR_157069.1:n.1040+39542G>C
(CCNH)
|
|
|
NR_157070.1:n.1204+39542G>C
(CCNH)
|
|
|
XM_011543525.2:c.1325C>G
(RASA1)
|
XP_011541827.1:p.Pro442Arg
|
|
XM_011543527.3:c.1325C>G
(RASA1)
|
XP_011541829.1:p.Pro442Arg
|
|
NM_001364075.2:c.934-40433G>C
(CCNH)
|
NP_001351004.1:n.934-40433G>C
|
|
NM_002890.3:c.1325C>G
(RASA1)
MANE Select
|
NP_002881.1:p.Pro442Arg
|
|
NR_157068.2:n.1447+39542G>C
(CCNH)
|
|
|
NR_157069.2:n.1040+39542G>C
(CCNH)
|
|
|
NR_157070.2:n.1204+39542G>C
(CCNH)
|
|
|
NM_022650.3:c.794C>G
(RASA1)
|
NP_072179.1:p.Pro265Arg
|
|