ENST00000281182.9:c.1195+317T>C
MANE Select
|
ENSP00000281182.5:n.1195+317T>C
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|
ENST00000281182.8:c.1195+317T>C
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ENSP00000281182.4:n.1195+317T>C
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|
ENST00000374752.6:c.814+317T>C
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ENSP00000363884.4:n.814+317T>C
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|
ENST00000524502.2:n.365T>C
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|
|
ENST00000526026.5:c.*1054T>C
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ENSP00000431532.1:n.*1054T>C
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|
ENST00000531338.5:n.1756T>C
|
|
|
ENST00000533387.5:n.2254+317T>C
|
|
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NM_014384.2:c.1195+317T>C , LRG_448t1:c.1195+317T>C
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NP_055199.1:n.1195+317T>C
|
|
XM_005271501.2:c.*60T>C
|
XP_005271558.1:n.*60T>C
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|
XM_011542750.1:c.1195+317T>C
|
XP_011541052.1:n.1195+317T>C
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|
XR_947819.1:n.1259+317T>C
|
|
|
XR_947820.1:n.1964T>C
|
|
|
XR_947822.1:n.1089+317T>C
|
|
|
XR_947823.1:n.1245+317T>C
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|
|
XM_005271505.4:c.*1460+317T>C
|
XP_005271562.1:n.*1460+317T>C
|
|
XM_011542750.3:c.1195+317T>C
|
XP_011541052.1:n.1195+317T>C
|
|
XM_017017542.2:c.1195+317T>C
|
XP_016873031.1:n.1195+317T>C
|
|
XM_017017543.2:c.*60T>C
|
XP_016873032.1:n.*60T>C
|
|
XM_017017544.2:c.*164+317T>C
|
XP_016873033.1:n.*164+317T>C
|
|
XM_017017545.2:c.*724T>C
|
XP_016873034.1:n.*724T>C
|
|
XM_017017546.2:c.901+317T>C
|
XP_016873035.1:n.901+317T>C
|
|
XM_017017547.2:c.901+317T>C
|
XP_016873036.1:n.901+317T>C
|
|
XM_017017548.2:c.*2001T>C
|
XP_016873037.1:n.*2001T>C
|
|
XM_017017549.2:c.*1605+317T>C
|
XP_016873038.1:n.*1605+317T>C
|
|
XM_024448437.1:c.*659T>C
|
XP_024304205.1:n.*659T>C
|
|
XM_024448438.1:c.814+317T>C
|
XP_024304206.1:n.814+317T>C
|
|
NM_014384.3:c.1195+317T>C
MANE Select
|
NP_055199.1:n.1195+317T>C
|
|