ENST00000494137.2:c.1277-140_1277-139insT
|
ENSP00000510626.1:n.1277-140_1277-139insT
|
|
ENST00000498257.6:c.1277-140_1277-139insT
|
ENSP00000510533.1:n.1277-140_1277-139insT
|
|
ENST00000617695.5:c.9200-140_9200-139insT
|
ENSP00000481744.2:n.9200-140_9200-139insT
|
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ENST00000618192.5:c.9476-140_9476-139insT
|
ENSP00000480802.2:n.9476-140_9476-139insT
|
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ENST00000688198.1:n.2190-140_2190-139insT
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|
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ENST00000688799.1:c.1277-140_1277-139insT
|
ENSP00000508458.1:n.1277-140_1277-139insT
|
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ENST00000690858.1:n.4085-140_4085-139insT
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|
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ENST00000693461.1:n.1549-140_1549-139insT
|
|
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ENST00000421865.3:c.9212-140_9212-139insT
MANE Select
|
ENSP00000400365.2:n.9212-140_9212-139insT
|
|
ENST00000421865.2:c.9212-140_9212-139insT
|
ENSP00000400365.2:n.9212-140_9212-139insT
|
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ENST00000617695.4:c.9200-140_9200-139insT
|
ENSP00000481744.1:n.9200-140_9200-139insT
|
|
ENST00000618192.4:c.9209-140_9209-139insT
|
ENSP00000480802.1:n.9209-140_9209-139insT
|
|
NM_000426.3:c.9212-140_9212-139insT , LRG_409t1:c.9212-140_9212-139insT
|
NP_000417.2:n.9212-140_9212-139insT
|
|
NM_001079823.1:c.9200-140_9200-139insT
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NP_001073291.1:n.9200-140_9200-139insT
|
|
XM_005266981.2:c.9476-140_9476-139insT
|
XP_005267038.1:n.9476-140_9476-139insT
|
|
XM_005266982.2:c.9464-140_9464-139insT
|
XP_005267039.1:n.9464-140_9464-139insT
|
|
XM_011535820.1:c.9470-140_9470-139insT
|
XP_011534122.1:n.9470-140_9470-139insT
|
|
XR_942984.1:n.1460+6426_1460+6427insA
|
|
|
XR_942985.1:n.1324+6426_1324+6427insA
|
|
|
XM_005266981.3:c.9476-140_9476-139insT
|
XP_005267038.1:n.9476-140_9476-139insT
|
|
XM_005266982.3:c.9464-140_9464-139insT
|
XP_005267039.1:n.9464-140_9464-139insT
|
|
XM_011535820.2:c.9470-140_9470-139insT
|
XP_011534122.1:n.9470-140_9470-139insT
|
|
XM_017010851.2:c.9482-140_9482-139insT
|
XP_016866340.1:n.9482-140_9482-139insT
|
|
XM_017010852.1:c.7607-140_7607-139insT
|
XP_016866341.1:n.7607-140_7607-139insT
|
|
XR_001743859.1:n.3900+6426_3900+6427insA
|
|
|
XR_001743860.1:n.1179+6426_1179+6427insA
|
|
|
XR_001743861.1:n.1346+6426_1346+6427insA
|
|
|
XR_001743863.1:n.883-13260_883-13259insA
|
|
|
XR_002956395.1:n.9131+6426_9131+6427insA
|
|
|
XR_002956396.1:n.3126+6426_3126+6427insA
|
|
|
NM_000426.4:c.9212-140_9212-139insT
MANE Select
|
NP_000417.3:n.9212-140_9212-139insT
|
|
NM_001079823.2:c.9200-140_9200-139insT
|
NP_001073291.2:n.9200-140_9200-139insT
|
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