ENST00000253778.13:c.1842+758A>C
MANE Select
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ENSP00000253778.8:n.1842+758A>C
|
|
ENST00000253778.12:c.1842+758A>C
|
ENSP00000253778.8:n.1842+758A>C
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|
NM_005110.2:c.1842+758A>C
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NP_005101.1:n.1842+758A>C
|
|
XM_006714942.1:c.1842+758A>C
|
XP_006715005.1:n.1842+758A>C
|
|
NM_005110.3:c.1842+758A>C
|
NP_005101.1:n.1842+758A>C
|
|
XM_006714942.2:c.1842+758A>C
|
XP_006715005.1:n.1842+758A>C
|
|
XM_017010100.2:c.1317+758A>C
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XP_016865589.1:n.1317+758A>C
|
|
XR_001742394.1:n.2366+758A>C
|
|
|
NM_005110.4:c.1842+758A>C
MANE Select
|
NP_005101.1:n.1842+758A>C
|
|