ENST00000367615.9:c.738+425A>G
MANE Select
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ENSP00000356587.4:n.738+425A>G
|
|
ENST00000367615.8:c.738+425A>G
|
ENSP00000356587.4:n.738+425A>G
|
|
ENST00000367616.4:c.535-2071A>G
|
ENSP00000356588.4:n.535-2071A>G
|
|
NM_001297575.1:c.535-2071A>G
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NP_001284504.1:n.535-2071A>G
|
|
NM_014625.3:c.738+425A>G , LRG_887t1:c.738+425A>G
|
NP_055440.1:n.738+425A>G
|
|
XM_005245483.2:c.561+425A>G
|
XP_005245540.1:n.561+425A>G
|
|
XM_006711529.2:c.738+425A>G
|
XP_006711592.1:n.738+425A>G
|
|
XM_005245483.3:c.561+425A>G
|
XP_005245540.1:n.561+425A>G
|
|
XM_017002298.1:c.461+3077A>G
|
XP_016857787.1:n.461+3077A>G
|
|
XM_017002299.1:c.534+3077A>G
|
XP_016857788.1:n.534+3077A>G
|
|
NM_001297575.2:c.535-2071A>G
|
NP_001284504.1:n.535-2071A>G
|
|
NM_014625.4:c.738+425A>G
MANE Select
|
NP_055440.1:n.738+425A>G
|
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