ENST00000399503.4:c.753T>A
MANE Select
|
ENSP00000382423.3:p.Pro251=
|
|
ENST00000399503.3:c.753T>A
|
ENSP00000382423.3:p.Pro251=
|
|
NM_005921.1:c.753T>A
|
NP_005912.1:p.Pro251=
|
|
XM_005248519.3:c.375T>A
|
XP_005248576.2:p.Pro125=
|
|
XM_011543406.1:c.498T>A
|
XP_011541708.1:p.Pro166=
|
|
XM_011543407.1:c.753T>A
|
XP_011541709.1:p.Pro251=
|
|
XM_011543408.1:c.753T>A
|
XP_011541710.1:p.Pro251=
|
|
XM_017009484.1:c.342T>A
|
XP_016864973.1:p.Pro114=
|
|
XM_017009485.1:c.264T>A
|
XP_016864974.1:p.Pro88=
|
|
XR_001742068.2:n.784T>A
|
|
|
NM_005921.2:c.753T>A
MANE Select
|
NP_005912.1:p.Pro251=
|
|