ENST00000333681.5:c.585+38256_585+38257delinsGA
MANE Select
|
ENSP00000329623.3:n.585+38256_585+38257delinsGA
|
|
ENST00000677227.1:c.913+1061_913+1062delinsGA
|
ENSP00000504566.1:n.913+1061_913+1062delinsGA
|
|
ENST00000678134.1:c.789+21836_789+21837delinsGA
|
ENSP00000503628.1:n.789+21836_789+21837delinsGA
|
|
ENST00000678349.1:c.1137+37704_1137+37705delinsGA
|
ENSP00000504190.1:n.1137+37704_1137+37705delinsGA
|
|
ENST00000333681.4:c.585+38256_585+38257delinsGA
|
ENSP00000329623.3:n.585+38256_585+38257delinsGA
|
|
ENST00000398117.1:c.585+38256_585+38257delinsGA
|
ENSP00000381185.1:n.585+38256_585+38257delinsGA
|
|
NM_000633.2:c.585+38256_585+38257delinsGA
|
NP_000624.2:n.585+38256_585+38257delinsGA
|
|
XR_935246.1:n.2025+1061_2025+1062delinsGA
|
|
|
XR_935247.1:n.2025+1061_2025+1062delinsGA
|
|
|
XR_935248.1:n.1804+1061_1804+1062delinsGA
|
|
|
XR_935248.3:n.2306+1061_2306+1062delinsGA
|
|
|
NM_000633.3:c.585+38256_585+38257delinsGA
MANE Select
|
NP_000624.2:n.585+38256_585+38257delinsGA
|
|