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ENST00000394867.9:n.1486-212_1486-211insCAGAACAGAGCAGCCACTC
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ENST00000688002.1:n.3198-212_3198-211insCAGAACAGAGCAGCCACTC
|
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ENST00000688751.1:n.183-212_183-211insCAGAACAGAGCAGCCACTC
|
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ENST00000689792.1:n.951-212_951-211insCAGAACAGAGCAGCCACTC
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ENST00000262948.10:c.1047-212_1047-211insCAGAACAGAGCAGCCACTC
MANE Select
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ENSP00000262948.4:n.1047-212_1047-211insCAGAACAGAGCAGCCACTC
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ENST00000262948.9:c.1047-212_1047-211insCAGAACAGAGCAGCCACTC
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ENSP00000262948.3:n.1047-212_1047-211insCAGAACAGAGCAGCCACTC
|
|
|
ENST00000394867.8:c.756-212_756-211insCAGAACAGAGCAGCCACTC
|
ENSP00000378336.1:n.756-212_756-211insCAGAACAGAGCAGCCACTC
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|
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ENST00000597263.5:n.232-212_232-211insCAGAACAGAGCAGCCACTC
|
|
|
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ENST00000599021.1:c.157-212_157-211insCAGAACAGAGCAGCCACTC
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ENST00000600584.5:n.2284_2285insCAGAACAGAGCAGCCACTC
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ENST00000601786.5:n.1348-212_1348-211insCAGAACAGAGCAGCCACTC
|
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NM_030662.3:c.1047-212_1047-211insCAGAACAGAGCAGCCACTC , LRG_750t1:c.1047-212_1047-211insCAGAACAGAGCAGCCACTC
|
NP_109587.1:n.1047-212_1047-211insCAGAACAGAGCAGCCACTC
|
|
|
XM_006722799.2:c.768-212_768-211insCAGAACAGAGCAGCCACTC
|
XP_006722862.1:n.768-212_768-211insCAGAACAGAGCAGCCACTC
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|
|
XM_011528133.1:c.477-212_477-211insCAGAACAGAGCAGCCACTC
|
XP_011526435.1:n.477-212_477-211insCAGAACAGAGCAGCCACTC
|
|
|
XM_017026989.1:c.1383_1384insCAGAACAGAGCAGCCACTC
|
XP_016882478.1:p.Cys462GlnfsTer?
|
|
|
XM_017026990.1:c.1104_1105insCAGAACAGAGCAGCCACTC
|
XP_016882479.1:p.Cys369GlnfsTer?
|
|
|
NM_030662.4:c.1047-212_1047-211insCAGAACAGAGCAGCCACTC
MANE Select
|
NP_109587.1:n.1047-212_1047-211insCAGAACAGAGCAGCCACTC
|
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