ENST00000333681.5:c.585+38121T>A
MANE Select
|
ENSP00000329623.3:n.585+38121T>A
|
|
ENST00000677227.1:c.913+926T>A
|
ENSP00000504566.1:n.913+926T>A
|
|
ENST00000678134.1:c.789+21701T>A
|
ENSP00000503628.1:n.789+21701T>A
|
|
ENST00000678349.1:c.1137+37569T>A
|
ENSP00000504190.1:n.1137+37569T>A
|
|
ENST00000333681.4:c.585+38121T>A
|
ENSP00000329623.3:n.585+38121T>A
|
|
ENST00000398117.1:c.585+38121T>A
|
ENSP00000381185.1:n.585+38121T>A
|
|
NM_000633.2:c.585+38121T>A
|
NP_000624.2:n.585+38121T>A
|
|
XR_935246.1:n.2025+926T>A
|
|
|
XR_935247.1:n.2025+926T>A
|
|
|
XR_935248.1:n.1804+926T>A
|
|
|
XR_935248.3:n.2306+926T>A
|
|
|
NM_000633.3:c.585+38121T>A
MANE Select
|
NP_000624.2:n.585+38121T>A
|
|