ENST00000355832.10:c.3983+353A>G
MANE Select
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ENSP00000348089.5:n.3983+353A>G
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ENST00000679552.1:n.1054+353A>G
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|
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ENST00000679871.1:n.1129+353A>G
|
|
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ENST00000679974.1:n.1032+353A>G
|
|
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ENST00000681632.1:n.5386+353A>G
|
|
|
ENST00000681659.1:c.3824+353A>G
|
ENSP00000505631.1:n.3824+353A>G
|
|
ENST00000355832.9:c.3983+353A>G
|
ENSP00000348089.5:n.3983+353A>G
|
|
ENST00000465653.1:n.305+353A>G
|
|
|
ENST00000623073.3:c.*2279+353A>G
|
ENSP00000485650.1:n.*2279+353A>G
|
|
ENST00000623115.3:c.2093+353A>G
|
ENSP00000485321.1:n.2093+353A>G
|
|
ENST00000624341.3:c.1815+353A>G
|
|
|
NM_000124.3:c.3983+353A>G
|
NP_000115.1:n.3983+353A>G
|
|
XR_945953.1:n.243-10566T>C
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|
|
NM_001346440.1:c.3983+353A>G
|
NP_001333369.1:n.3983+353A>G
|
|
NM_000124.4:c.3983+353A>G
MANE Select
|
NP_000115.1:n.3983+353A>G
|
|
NM_001346440.2:c.3983+353A>G
|
NP_001333369.1:n.3983+353A>G
|
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