NM_022095.4:c.3332G>T
MANE Select
|
NP_071378.1:p.Arg1111Leu
|
ENST00000322927.3:c.3332G>T
MANE Select
|
ENSP00000325326.2:p.Arg1111Leu
|
NM_022095.3:c.3332G>T
|
NP_071378.1:p.Arg1111Leu
|
ENST00000322927.2:c.3332G>T
|
ENSP00000325326.2:p.Arg1111Leu
|
XM_005260504.3:c.3329G>T
|
XP_005260561.1:p.Arg1110Leu
|
XM_005260504.4:c.3329G>T
|
XP_005260561.1:p.Arg1110Leu
|
XM_005260506.2:c.2804G>T
|
XP_005260563.1:p.Arg935Leu
|
XM_017028012.1:c.2804G>T
|
XP_016883501.1:p.Arg935Leu
|
XR_002958500.1:n.5279G>T
|
|
XR_002958501.1:n.3728G>T
|
|
XR_936602.3:n.3843G>T
|
|