ENST00000622633.5:c.221-48G>T
MANE Select
|
ENSP00000483114.1:n.221-48G>T
|
|
ENST00000339430.9:c.221-48G>T
|
ENSP00000340118.5:n.221-48G>T
|
|
ENST00000381810.7:c.221-48G>T
|
ENSP00000371231.3:n.221-48G>T
|
|
ENST00000413364.6:c.221-48G>T
|
ENSP00000397958.2:n.221-48G>T
|
|
ENST00000570798.5:c.221-48G>T
|
ENSP00000458871.1:n.221-48G>T
|
|
ENST00000570904.5:c.221-48G>T
|
ENSP00000459138.1:n.221-48G>T
|
|
ENST00000571459.5:c.220+2774G>T
|
ENSP00000459603.1:n.220+2774G>T
|
|
ENST00000571627.5:c.221-48G>T
|
ENSP00000460743.1:n.221-48G>T
|
|
ENST00000571688.5:c.221-48G>T
|
ENSP00000459533.1:n.221-48G>T
|
|
ENST00000571976.1:c.221-48G>T
|
ENSP00000460133.1:n.221-48G>T
|
|
ENST00000572255.5:c.-59-48G>T
|
ENSP00000458836.1:n.-59-48G>T
|
|
ENST00000573332.5:c.232G>T
|
ENSP00000460873.1:p.Gly78Cys
|
|
ENST00000574701.5:c.221-48G>T
|
ENSP00000458981.1:n.221-48G>T
|
|
ENST00000574763.5:c.221-48G>T
|
ENSP00000461813.1:n.221-48G>T
|
|
ENST00000575426.1:c.40-48G>T
|
|
|
ENST00000576036.5:c.221-48G>T
|
ENSP00000461667.1:n.221-48G>T
|
|
ENST00000620789.4:c.221-48G>T
|
ENSP00000481589.1:n.221-48G>T
|
|
ENST00000622633.4:c.221-48G>T
|
ENSP00000483114.1:n.221-48G>T
|
|
NM_001136472.1:c.221-48G>T
|
NP_001129944.1:n.221-48G>T
|
|
NM_001136473.1:c.221-48G>T , LRG_253t1:c.221-48G>T
|
NP_001129945.1:n.221-48G>T
|
|
NM_004862.3:c.221-48G>T
|
NP_004853.2:n.221-48G>T
|
|
NR_024320.1:n.355-48G>T
|
|
|
XM_006720982.2:c.221-48G>T
|
XP_006721045.1:n.221-48G>T
|
|
XM_006720983.2:c.221-48G>T
|
XP_006721046.1:n.221-48G>T
|
|
XM_006720984.2:c.221-48G>T
|
XP_006721047.1:n.221-48G>T
|
|
XM_006720985.2:c.221-48G>T
|
XP_006721048.1:n.221-48G>T
|
|
XM_011522754.1:c.311-48G>T
|
XP_011521056.1:n.311-48G>T
|
|
XM_006720982.3:c.221-48G>T
|
XP_006721045.1:n.221-48G>T
|
|
XM_006720983.4:c.221-48G>T
|
XP_006721046.1:n.221-48G>T
|
|
XM_006720984.4:c.221-48G>T
|
XP_006721047.1:n.221-48G>T
|
|
XM_006720985.3:c.221-48G>T
|
XP_006721048.1:n.221-48G>T
|
|
XM_011522754.3:c.311-48G>T
|
XP_011521056.1:n.311-48G>T
|
|
XM_017023896.1:c.221-48G>T
|
XP_016879385.1:n.221-48G>T
|
|
NM_001136472.2:c.221-48G>T
MANE Select
|
NP_001129944.1:n.221-48G>T
|
|
NM_004862.4:c.221-48G>T
|
NP_004853.2:n.221-48G>T
|
|
NR_024320.2:n.355-48G>T
|
|
|