ENST00000682565.1:c.10449G>T
|
ENSP00000507671.1:p.Arg3483Ser
|
|
ENST00000682801.1:c.10449G>T
|
ENSP00000507862.1:p.Arg3483Ser
|
|
ENST00000682859.1:c.10449G>T
|
ENSP00000508222.1:p.Arg3483Ser
|
|
ENST00000683791.1:c.3535G>T
|
|
|
ENST00000684460.1:c.7730G>T
|
|
|
ENST00000684548.1:c.10449G>T
|
ENSP00000507421.1:p.Arg3483Ser
|
|
ENST00000684590.1:c.4896G>T
|
ENSP00000507376.1:p.Arg1632Ser
|
|
ENST00000684656.1:c.7775G>T
|
|
|
ENST00000613296.6:c.10830G>T
MANE Select
|
ENSP00000482968.1:p.Arg3610Ser
|
|
ENST00000651057.1:c.984G>T
|
ENSP00000498504.1:p.Arg328Ser
|
|
ENST00000651434.1:c.2186G>T
|
|
|
ENST00000651750.1:c.218G>T
|
|
|
ENST00000652487.1:c.1927G>T
|
|
|
ENST00000423048.5:c.4321G>T
|
ENSP00000399833.1:n.4321G>T
|
|
ENST00000484298.5:c.10704G>T
|
ENSP00000478155.1:p.Arg3568Ser
|
|
ENST00000613296.4:c.10830G>T
|
ENSP00000482968.1:p.Arg3610Ser
|
|
ENST00000614410.4:c.10830G>T
|
ENSP00000479094.1:p.Arg3610Ser
|
|
ENST00000620466.4:n.4633G>T
|
|
|
NM_015120.4:c.10833G>T , LRG_741t1:c.10833G>T
|
NP_055935.4:p.Arg3611Ser
|
|
NM_001378454.1:c.10830G>T
MANE Select
|
NP_001365383.1:p.Arg3610Ser
|
|