ENST00000274376.11:c.2967G>T
(RASA1)
MANE Select
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ENSP00000274376.6:p.Thr989=
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ENST00000645953.1:c.*90+3336C>A
(CCNH)
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ENSP00000494460.1:n.*90+3336C>A
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ENST00000646883.1:c.254+3336C>A
(CCNH)
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ENST00000274376.10:c.2967G>T
(RASA1)
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ENSP00000274376.6:p.Thr989=
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ENST00000456692.6:c.2436G>T
(RASA1)
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ENSP00000411221.2:p.Thr812=
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ENST00000506290.1:c.2469G>T
(RASA1)
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ENSP00000420905.1:p.Thr823=
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ENST00000512763.5:c.2466G>T
(RASA1)
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ENSP00000422008.1:p.Thr822=
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ENST00000515800.6:c.*1582G>T
(RASA1)
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ENSP00000423395.2:n.*1582G>T
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NM_002890.2:c.2967G>T
(RASA1)
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NP_002881.1:p.Thr989=
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NM_022650.2:c.2436G>T
(RASA1)
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NP_072179.1:p.Thr812=
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XM_011543525.1:c.2880G>T
(RASA1)
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XP_011541827.1:p.Thr960=
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NM_001364075.1:c.933+5610C>A
(CCNH)
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NP_001351004.1:n.933+5610C>A
|
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NR_157068.1:n.1447+3336C>A
(CCNH)
|
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NR_157069.1:n.1040+3336C>A
(CCNH)
|
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NR_157070.1:n.1204+3336C>A
(CCNH)
|
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XM_011543525.2:c.2880G>T
(RASA1)
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XP_011541827.1:p.Thr960=
|
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NM_001364075.2:c.933+5610C>A
(CCNH)
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NP_001351004.1:n.933+5610C>A
|
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NM_002890.3:c.2967G>T
(RASA1)
MANE Select
|
NP_002881.1:p.Thr989=
|
|
NR_157068.2:n.1447+3336C>A
(CCNH)
|
|
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NR_157069.2:n.1040+3336C>A
(CCNH)
|
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NR_157070.2:n.1204+3336C>A
(CCNH)
|
|
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NM_022650.3:c.2436G>T
(RASA1)
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NP_072179.1:p.Thr812=
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