ENST00000053867.8:c.1414-17_1414-12delinsGCTCCC
MANE Select
|
ENSP00000053867.2:n.1414-17_1414-12delinsGCTCCC
|
|
ENST00000639447.1:c.1137-205_1137-200delinsGCTCCC
|
ENSP00000492014.1:n.1137-205_1137-200delinsGCTCCC
|
|
ENST00000053867.7:c.1414-17_1414-12delinsGCTCCC
|
ENSP00000053867.2:n.1414-17_1414-12delinsGCTCCC
|
|
ENST00000586242.1:c.48-17_48-12delinsGCTCCC
|
|
|
ENST00000586443.1:c.855-17_855-12delinsGCTCCC
|
|
|
ENST00000589265.5:c.943-17_943-12delinsGCTCCC
|
ENSP00000467616.1:n.943-17_943-12delinsGCTCCC
|
|
NM_002087.3:c.1414-17_1414-12delinsGCTCCC
|
NP_002078.1:n.1414-17_1414-12delinsGCTCCC
|
|
XM_005257253.1:c.1414-17_1414-12delinsGCTCCC
|
XP_005257310.1:n.1414-17_1414-12delinsGCTCCC
|
|
XM_024450730.1:c.1414-17_1414-12delinsGCTCCC
|
XP_024306498.1:n.1414-17_1414-12delinsGCTCCC
|
|
NM_002087.4:c.1414-17_1414-12delinsGCTCCC
MANE Select
|
NP_002078.1:n.1414-17_1414-12delinsGCTCCC
|
|