ENST00000333371.8:c.-202G>T
MANE Select
|
ENSP00000327650.4:n.-202G>T
|
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ENST00000643536.1:c.-202G>T
|
ENSP00000494429.1:n.-202G>T
|
|
ENST00000333371.7:c.-202G>T
|
ENSP00000327650.3:n.-202G>T
|
|
ENST00000535906.1:c.-202G>T
|
ENSP00000444053.1:n.-202G>T
|
|
ENST00000556096.6:n.153G>T
|
|
|
ENST00000557358.1:n.146G>T
|
|
|
ENST00000574755.5:c.-202G>T
|
ENSP00000460413.1:n.-202G>T
|
|
NM_001289148.1:c.-202G>T
|
NP_001276077.1:n.-202G>T
|
|
NM_001289149.1:c.-413G>T
|
NP_001276078.1:n.-413G>T
|
|
NM_018668.4:c.-202G>T , LRG_884t1:c.-202G>T
|
NP_061138.3:n.-202G>T
|
|
XM_005254884.2:c.-202G>T
|
XP_005254941.1:n.-202G>T
|
|
XM_005254887.1:c.-332G>T
|
XP_005254944.1:n.-332G>T
|
|
XM_005254888.2:c.-202G>T
|
XP_005254945.1:n.-202G>T
|
|
XM_011521448.1:c.-515G>T
|
XP_011519750.1:n.-515G>T
|
|
XM_017022075.2:c.-563G>T
|
XP_016877564.1:n.-563G>T
|
|
XM_017022076.1:c.-420G>T
|
XP_016877565.1:n.-420G>T
|
|
XR_001751213.2:n.135G>T
|
|
|
NM_018668.5:c.-202G>T
MANE Select
|
NP_061138.3:n.-202G>T
|
|