ENST00000264613.11:c.2915T>G
MANE Select
|
ENSP00000264613.6:p.Leu972Arg
|
|
ENST00000264613.10:c.2915T>G
|
ENSP00000264613.6:p.Leu972Arg
|
|
ENST00000460674.5:n.832T>G
|
|
|
ENST00000463556.5:n.437T>G
|
|
|
ENST00000479771.5:c.320T>G
|
ENSP00000420367.1:p.Leu107Arg
|
|
ENST00000481169.5:c.2702T>G
|
ENSP00000418773.1:p.Leu901Arg
|
|
ENST00000490639.5:n.2947T>G
|
|
|
ENST00000494544.1:c.2264T>G
|
ENSP00000420545.1:p.Leu755Arg
|
|
NM_000096.3:c.2915T>G
|
NP_000087.1:p.Leu972Arg
|
|
NR_046371.1:n.2955T>G
|
|
|
XM_006713499.2:c.2915T>G
|
XP_006713562.1:p.Leu972Arg
|
|
XM_006713500.2:c.2915T>G
|
XP_006713563.1:p.Leu972Arg
|
|
XM_006713501.2:c.2915T>G
|
XP_006713564.1:p.Leu972Arg
|
|
XM_011512435.1:c.2915T>G
|
XP_011510737.1:p.Leu972Arg
|
|
XR_427361.2:n.3173T>G
|
|
|
XM_006713499.3:c.2915T>G
|
XP_006713562.1:p.Leu972Arg
|
|
XM_006713500.4:c.2915T>G
|
XP_006713563.1:p.Leu972Arg
|
|
XM_006713501.3:c.2915T>G
|
XP_006713564.1:p.Leu972Arg
|
|
XM_011512435.2:c.2915T>G
|
XP_011510737.1:p.Leu972Arg
|
|
XM_017005734.2:c.2915T>G
|
XP_016861223.1:p.Leu972Arg
|
|
XM_017005735.2:c.2915T>G
|
XP_016861224.1:p.Leu972Arg
|
|
XR_427361.3:n.3131T>G
|
|
|
NM_000096.4:c.2915T>G
MANE Select
|
NP_000087.2:p.Leu972Arg
|
|
NR_046371.2:n.2739T>G
|
|
|