ENST00000539696.6:c.197-148_197-147insTTCGACTCT
|
ENSP00000439134.1:n.197-148_197-147insTTCGACTCT
|
|
ENST00000546277.6:c.1040-148_1040-147insTTCGACTCT
|
ENSP00000438153.2:n.1040-148_1040-147insTTCGACTCT
|
|
ENST00000636529.2:n.679-148_679-147insTTCGACTCT
|
|
|
ENST00000697195.1:c.*804-148_*804-147insTTCGACTCT
|
ENSP00000513181.1:n.*804-148_*804-147insTTCGACTCT
|
|
ENST00000697196.1:c.*213-148_*213-147insTTCGACTCT
|
ENSP00000513182.1:n.*213-148_*213-147insTTCGACTCT
|
|
ENST00000697197.1:n.3069-148_3069-147insTTCGACTCT
|
|
|
ENST00000697198.1:n.1424-148_1424-147insTTCGACTCT
|
|
|
ENST00000228510.8:c.1040-148_1040-147insTTCGACTCT
MANE Select
|
ENSP00000228510.3:n.1040-148_1040-147insTTCGACTCT
|
|
ENST00000636529.1:c.665-148_665-147insTTCGACTCT
|
|
|
ENST00000636996.1:c.888-148_888-147insTTCGACTCT
|
|
|
ENST00000228510.7:c.1040-148_1040-147insTTCGACTCT
|
ENSP00000228510.3:n.1040-148_1040-147insTTCGACTCT
|
|
ENST00000392727.7:c.884-148_884-147insTTCGACTCT
|
ENSP00000376487.3:n.884-148_884-147insTTCGACTCT
|
|
ENST00000447878.6:c.*487-148_*487-147insTTCGACTCT
|
ENSP00000415555.2:n.*487-148_*487-147insTTCGACTCT
|
|
ENST00000537237.5:c.*713-148_*713-147insTTCGACTCT
|
ENSP00000445382.1:n.*713-148_*713-147insTTCGACTCT
|
|
ENST00000539575.4:c.1040-148_1040-147insTTCGACTCT
|
ENSP00000443551.2:n.1040-148_1040-147insTTCGACTCT
|
|
ENST00000539696.5:c.197-148_197-147insTTCGACTCT
|
ENSP00000439134.1:n.197-148_197-147insTTCGACTCT
|
|
ENST00000540353.1:n.3273-148_3273-147insTTCGACTCT
|
|
|
ENST00000625889.2:c.884-148_884-147insTTCGACTCT
|
ENSP00000486846.1:n.884-148_884-147insTTCGACTCT
|
|
ENST00000629016.2:c.*487-148_*487-147insTTCGACTCT
|
ENSP00000486804.1:n.*487-148_*487-147insTTCGACTCT
|
|
NM_000431.3:c.1040-148_1040-147insTTCGACTCT
|
NP_000422.1:n.1040-148_1040-147insTTCGACTCT
|
|
NM_001114185.2:c.1040-148_1040-147insTTCGACTCT
|
NP_001107657.1:n.1040-148_1040-147insTTCGACTCT
|
|
NM_001301182.1:c.884-148_884-147insTTCGACTCT
|
NP_001288111.1:n.884-148_884-147insTTCGACTCT
|
|
XM_011538372.1:c.1040-148_1040-147insTTCGACTCT
|
XP_011536674.1:n.1040-148_1040-147insTTCGACTCT
|
|
XM_017019313.2:c.884-148_884-147insTTCGACTCT
|
XP_016874802.1:n.884-148_884-147insTTCGACTCT
|
|
XM_017019314.1:c.1040-148_1040-147insTTCGACTCT
|
XP_016874803.1:n.1040-148_1040-147insTTCGACTCT
|
|
NM_000431.4:c.1040-148_1040-147insTTCGACTCT
MANE Select
|
NP_000422.1:n.1040-148_1040-147insTTCGACTCT
|
|
NM_001114185.3:c.1040-148_1040-147insTTCGACTCT
|
NP_001107657.1:n.1040-148_1040-147insTTCGACTCT
|
|
NM_001301182.2:c.884-148_884-147insTTCGACTCT
|
NP_001288111.1:n.884-148_884-147insTTCGACTCT
|
|