ENST00000261381.7:c.1764+121_1764+122insTG
MANE Select
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ENSP00000261381.6:n.1764+121_1764+122insTG
|
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ENST00000261381.6:c.1764+121_1764+122insTG
|
ENSP00000261381.6:n.1764+121_1764+122insTG
|
|
NM_022166.3:c.1764+121_1764+122insTG
|
NP_071449.1:n.1764+121_1764+122insTG
|
|
XM_011522574.1:c.1764+121_1764+122insTG
|
XP_011520876.1:n.1764+121_1764+122insTG
|
|
XR_933140.1:n.336-9_336-8insCA
|
|
|
XR_933141.1:n.175-9_175-8insCA
|
|
|
XR_933143.1:n.237-9_237-8insCA
|
|
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NR_135179.1:n.147-9_147-8insCA
|
|
|
XM_017023539.2:c.1764+121_1764+122insTG
|
XP_016879028.1:n.1764+121_1764+122insTG
|
|
XM_017023540.2:c.1764+121_1764+122insTG
|
XP_016879029.1:n.1764+121_1764+122insTG
|
|
NM_022166.4:c.1764+121_1764+122insTG
MANE Select
|
NP_071449.1:n.1764+121_1764+122insTG
|
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