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ENST00000703118.1:c.*2742-1172_*2742-1159delinsGGACAGCCAGTTCT
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ENSP00000515181.1:n.*2742-1172_*2742-1159delinsGGACAGCCAGTTCT...
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|
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ENST00000703131.1:n.3285-1172_3285-1159delinsGGACAGCCAGTTCT
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|
|
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ENST00000703139.1:c.2155-1172_2155-1159delinsGGACAGCCAGTTCT
|
|
|
|
ENST00000703140.1:c.7154-1172_7154-1159delinsGGACAGCCAGTTCT
|
ENSP00000515197.1:n.7154-1172_7154-1159delinsGGACAGCCAGTTCT
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|
|
ENST00000703141.1:c.*2884-1172_*2884-1159delinsGGACAGCCAGTTCT
|
ENSP00000515198.1:n.*2884-1172_*2884-1159delinsGGACAGCCAGTTCT...
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|
|
ENST00000703142.1:c.*4197-1172_*4197-1159delinsGGACAGCCAGTTCT
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ENSP00000515199.1:n.*4197-1172_*4197-1159delinsGGACAGCCAGTTCT...
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|
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ENST00000361445.9:c.7367-1172_7367-1159delinsGGACAGCCAGTTCT
MANE Select
|
ENSP00000354558.4:n.7367-1172_7367-1159delinsGGACAGCCAGTTCT
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|
|
ENST00000361445.8:c.7367-1172_7367-1159delinsGGACAGCCAGTTCT
|
ENSP00000354558.4:n.7367-1172_7367-1159delinsGGACAGCCAGTTCT
|
|
|
ENST00000376838.5:c.1982-1172_1982-1159delinsGGACAGCCAGTTCT
|
ENSP00000366034.1:n.1982-1172_1982-1159delinsGGACAGCCAGTTCT
|
|
|
ENST00000455339.1:c.335-1172_335-1159delinsGGACAGCCAGTTCT
|
ENSP00000398745.1:n.335-1172_335-1159delinsGGACAGCCAGTTCT
|
|
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ENST00000473471.5:n.379-1172_379-1159delinsGGACAGCCAGTTCT
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|
|
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ENST00000490931.1:n.649+613_649+626delinsGGACAGCCAGTTCT
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|
NM_004958.3:c.7367-1172_7367-1159delinsGGACAGCCAGTTCT , LRG_734t1:c.7367-1172_7367-1159delinsGGACAGCCAGTTCT
|
NP_004949.1:n.7367-1172_7367-1159delinsGGACAGCCAGTTCT
|
|
|
XM_005263438.1:c.7367-1172_7367-1159delinsGGACAGCCAGTTCT
|
XP_005263495.1:n.7367-1172_7367-1159delinsGGACAGCCAGTTCT
|
|
|
XM_005263438.2:c.7367-1172_7367-1159delinsGGACAGCCAGTTCT
|
XP_005263495.1:n.7367-1172_7367-1159delinsGGACAGCCAGTTCT
|
|
|
XM_017000900.1:c.6686-1172_6686-1159delinsGGACAGCCAGTTCT
|
XP_016856389.1:n.6686-1172_6686-1159delinsGGACAGCCAGTTCT
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|
|
XM_017000901.1:c.6119-1172_6119-1159delinsGGACAGCCAGTTCT
|
XP_016856390.1:n.6119-1172_6119-1159delinsGGACAGCCAGTTCT
|
|
|
XM_024446187.1:c.7367-1172_7367-1159delinsGGACAGCCAGTTCT
|
XP_024301955.1:n.7367-1172_7367-1159delinsGGACAGCCAGTTCT
|
|
|
XR_001737087.1:n.7405-1172_7405-1159delinsGGACAGCCAGTTCT
|
|
|
|
NM_004958.4:c.7367-1172_7367-1159delinsGGACAGCCAGTTCT
MANE Select
|
NP_004949.1:n.7367-1172_7367-1159delinsGGACAGCCAGTTCT
|
|
|
NM_001386500.1:c.7367-1172_7367-1159delinsGGACAGCCAGTTCT
|
NP_001373429.1:n.7367-1172_7367-1159delinsGGACAGCCAGTTCT
|
|
|
NM_001386501.1:c.6119-1172_6119-1159delinsGGACAGCCAGTTCT
|
NP_001373430.1:n.6119-1172_6119-1159delinsGGACAGCCAGTTCT
|
|
