ENST00000271751.10:c.1463-199G>A
MANE Select
|
ENSP00000271751.4:n.1463-199G>A
|
|
ENST00000367007.5:c.1382-199G>A
|
ENSP00000355974.5:n.1382-199G>A
|
|
ENST00000638357.1:c.796-199G>A
|
|
|
ENST00000638498.1:c.1463-199G>A
|
ENSP00000490983.1:n.1463-199G>A
|
|
ENST00000638960.1:c.1382-199G>A
|
ENSP00000492302.1:n.1382-199G>A
|
|
ENST00000639952.1:c.1382-199G>A
|
ENSP00000492697.1:n.1382-199G>A
|
|
ENST00000640044.1:c.311-199G>A
|
ENSP00000491434.1:n.311-199G>A
|
|
ENST00000640243.1:c.952-199G>A
|
ENSP00000492803.1:n.952-199G>A
|
|
ENST00000640522.1:c.1033-199G>A
|
ENSP00000491019.1:n.1033-199G>A
|
|
ENST00000640528.1:c.1382-199G>A
|
ENSP00000491725.1:n.1382-199G>A
|
|
ENST00000640566.1:c.311-28821G>A
|
ENSP00000491302.1:n.311-28821G>A
|
|
ENST00000640710.1:c.1382-199G>A
|
ENSP00000492513.1:n.1382-199G>A
|
|
ENST00000271751.8:c.1463-199G>A
|
ENSP00000271751.4:n.1463-199G>A
|
|
ENST00000367007.4:c.1382-199G>A
|
ENSP00000355974.4:n.1382-199G>A
|
|
NM_002238.3:c.1382-199G>A
|
NP_002229.1:n.1382-199G>A
|
|
NM_172362.2:c.1463-199G>A
|
NP_758872.1:n.1463-199G>A
|
|
XM_011509514.1:c.287-199G>A
|
XP_011507816.1:n.287-199G>A
|
|
XM_017001246.1:c.287-199G>A
|
XP_016856735.1:n.287-199G>A
|
|
NM_172362.3:c.1463-199G>A
MANE Select
|
NP_758872.1:n.1463-199G>A
|
|
NM_002238.4:c.1382-199G>A
|
NP_002229.1:n.1382-199G>A
|
|