ENST00000394867.9:n.1486-140_1486-139insG
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|
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ENST00000688002.1:n.3198-140_3198-139insG
|
|
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ENST00000688751.1:n.183-140_183-139insG
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ENST00000689792.1:n.951-140_951-139insG
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|
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ENST00000262948.10:c.1047-140_1047-139insG
MANE Select
|
ENSP00000262948.4:n.1047-140_1047-139insG
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ENST00000262948.9:c.1047-140_1047-139insG
|
ENSP00000262948.3:n.1047-140_1047-139insG
|
|
ENST00000394867.8:c.756-140_756-139insG
|
ENSP00000378336.1:n.756-140_756-139insG
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|
ENST00000597263.5:n.232-140_232-139insG
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ENST00000599021.1:c.157-140_157-139insG
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ENST00000600584.5:n.2356_2357insG
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|
|
ENST00000601786.5:n.1348-140_1348-139insG
|
|
|
NM_030662.3:c.1047-140_1047-139insG , LRG_750t1:c.1047-140_1047-139insG
|
NP_109587.1:n.1047-140_1047-139insG
|
|
XM_006722799.2:c.768-140_768-139insG
|
XP_006722862.1:n.768-140_768-139insG
|
|
XM_011528133.1:c.477-140_477-139insG
|
XP_011526435.1:n.477-140_477-139insG
|
|
XM_017026989.1:c.1455_1456insG
|
XP_016882478.1:p.Leu486AlafsTer?
|
|
XM_017026990.1:c.1176_1177insG
|
XP_016882479.1:p.Leu393AlafsTer?
|
|
NM_030662.4:c.1047-140_1047-139insG
MANE Select
|
NP_109587.1:n.1047-140_1047-139insG
|
|