ENST00000403231.6:c.1130-2278G>T
MANE Select
|
ENSP00000385808.1:n.1130-2278G>T
|
|
ENST00000378735.5:c.1130-2278G>T
|
ENSP00000368009.1:n.1130-2278G>T
|
|
ENST00000378746.8:c.1130-2278G>T
|
ENSP00000368020.3:n.1130-2278G>T
|
|
ENST00000403231.5:c.1130-2278G>T
|
ENSP00000385808.1:n.1130-2278G>T
|
|
ENST00000618515.4:c.1130-2281G>T
|
ENSP00000483023.1:n.1130-2281G>T
|
|
NM_001300791.1:c.1130-2278G>T
|
NP_001287720.1:n.1130-2278G>T
|
|
NM_001300792.1:c.1130-2278G>T
|
NP_001287721.1:n.1130-2278G>T
|
|
NM_007054.6:c.1130-2278G>T
|
NP_008985.3:n.1130-2278G>T
|
|
XM_006714526.2:c.1130-2278G>T
|
XP_006714589.1:n.1130-2278G>T
|
|
XM_006714526.4:c.1130-2278G>T
|
XP_006714589.1:n.1130-2278G>T
|
|
XM_017008995.2:c.1130-2278G>T
|
XP_016864484.1:n.1130-2278G>T
|
|
XM_017008996.2:c.1130-2278G>T
|
XP_016864485.1:n.1130-2278G>T
|
|
NM_001300791.2:c.1130-2278G>T
MANE Select
|
NP_001287720.1:n.1130-2278G>T
|
|
NM_001300792.2:c.1130-2278G>T
|
NP_001287721.1:n.1130-2278G>T
|
|
NM_007054.7:c.1130-2278G>T
|
NP_008985.3:n.1130-2278G>T
|
|