ENST00000053867.8:c.1179+105_1179+106insAG
MANE Select
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ENSP00000053867.2:n.1179+105_1179+106insAG
|
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ENST00000639447.1:c.1136+148_1136+149insAG
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ENSP00000492014.1:n.1136+148_1136+149insAG
|
|
ENST00000053867.7:c.1179+105_1179+106insAG
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ENSP00000053867.2:n.1179+105_1179+106insAG
|
|
ENST00000586443.1:c.620+105_620+106insAG
|
|
|
ENST00000589265.5:c.708+105_708+106insAG
|
ENSP00000467616.1:n.708+105_708+106insAG
|
|
NM_002087.3:c.1179+105_1179+106insAG
|
NP_002078.1:n.1179+105_1179+106insAG
|
|
XM_005257253.1:c.1179+105_1179+106insAG
|
XP_005257310.1:n.1179+105_1179+106insAG
|
|
XM_024450730.1:c.1179+105_1179+106insAG
|
XP_024306498.1:n.1179+105_1179+106insAG
|
|
NM_002087.4:c.1179+105_1179+106insAG
MANE Select
|
NP_002078.1:n.1179+105_1179+106insAG
|
|