ENST00000305264.8:c.1217+425T>A
MANE Select
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ENSP00000302967.3:n.1217+425T>A
|
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ENST00000305264.7:c.1217+425T>A
|
ENSP00000302967.3:n.1217+425T>A
|
|
ENST00000459727.5:n.471+425T>A
|
|
|
ENST00000469207.5:n.216+425T>A
|
|
|
ENST00000469550.6:n.1290+425T>A
|
|
|
NM_003883.3:c.1217+425T>A
|
NP_003874.2:n.1217+425T>A
|
|
XM_011537697.1:c.656+425T>A
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XP_011535999.1:n.656+425T>A
|
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XR_427789.2:n.231-1064A>T
|
|
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XR_944336.1:n.1302+425T>A
|
|
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NM_001355040.1:c.758+425T>A
|
NP_001341969.1:n.758+425T>A
|
|
NM_001355041.1:c.656+425T>A
|
NP_001341970.1:n.656+425T>A
|
|
NR_149164.1:n.1203+425T>A
|
|
|
NR_149165.1:n.1165+425T>A
|
|
|
NR_149166.1:n.1081+425T>A
|
|
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NR_149168.1:n.1308+425T>A
|
|
|
NR_149169.1:n.1228+425T>A
|
|
|
NM_003883.4:c.1217+425T>A
MANE Select
|
NP_003874.2:n.1217+425T>A
|
|
NM_001355040.2:c.758+425T>A
|
NP_001341969.1:n.758+425T>A
|
|
NM_001355041.2:c.656+425T>A
|
NP_001341970.1:n.656+425T>A
|
|
NR_149164.2:n.1196+425T>A
|
|
|
NR_149165.2:n.1158+425T>A
|
|
|
NR_149166.2:n.1074+425T>A
|
|
|
NR_149168.2:n.1301+425T>A
|
|
|
NR_149169.2:n.1221+425T>A
|
|
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