ENST00000361727.8:c.1777+6547A>T
MANE Select
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ENSP00000354778.3:n.1777+6547A>T
|
|
ENST00000636870.1:n.1639+6547A>T
|
|
|
ENST00000637694.1:n.1681-4033A>T
|
|
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ENST00000637825.1:n.1260+6547A>T
|
|
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ENST00000638117.1:n.1680+6547A>T
|
|
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ENST00000361727.7:c.1777+6547A>T
|
ENSP00000354778.3:n.1777+6547A>T
|
|
NM_014141.5:c.1777+6547A>T
|
NP_054860.1:n.1777+6547A>T
|
|
XM_006715919.1:c.265+6547A>T
|
XP_006715982.1:n.265+6547A>T
|
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XM_017011950.2:c.1777+6547A>T
|
XP_016867439.1:n.1777+6547A>T
|
|
NM_014141.6:c.1777+6547A>T
MANE Select
|
NP_054860.1:n.1777+6547A>T
|
|