|
ENST00000491895.7:c.747G>T
MANE Select
|
ENSP00000419045.2:p.Arg249Ser
|
|
|
ENST00000254299.8:n.895G>T
|
|
|
|
ENST00000395514.5:c.747G>T
|
ENSP00000378890.1:p.Arg249Ser
|
|
|
ENST00000395521.6:n.293-969G>T
|
|
|
|
ENST00000491895.6:c.747G>T
|
ENSP00000419045.2:p.Arg249Ser
|
|
|
ENST00000536224.2:c.627-969G>T
|
ENSP00000445246.2:n.627-969G>T
|
|
|
ENST00000543643.6:c.627-154G>T
|
ENSP00000444011.2:n.627-154G>T
|
|
|
ENST00000622544.4:c.747G>T
|
ENSP00000477796.1:p.Arg249Ser
|
|
|
NM_000161.2:c.747G>T
|
NP_000152.1:p.Arg249Ser
|
|
|
NM_001024024.1:c.747G>T
|
NP_001019195.1:p.Arg249Ser
|
|
|
NM_001024070.1:c.627-154G>T
|
NP_001019241.1:n.627-154G>T
|
|
|
NM_001024071.1:c.627-969G>T
|
NP_001019242.1:n.627-969G>T
|
|
|
XM_005267530.1:c.627-154G>T
|
XP_005267587.1:n.627-154G>T
|
|
|
XM_017021218.1:c.453G>T
|
XP_016876707.1:p.Arg151Ser
|
|
|
NM_000161.3:c.747G>T
MANE Select
|
NP_000152.1:p.Arg249Ser
|
|
|
NM_001024070.2:c.627-154G>T
|
NP_001019241.1:n.627-154G>T
|
|
|
NM_001024071.2:c.627-969G>T
|
NP_001019242.1:n.627-969G>T
|
|
|
NM_001024024.2:c.747G>T
|
NP_001019195.1:p.Arg249Ser
|
|
