ENST00000405440.7:c.709C>T
MANE Select
|
ENSP00000384152.3:p.Arg237Trp
|
|
ENST00000310346.8:c.709C>T
|
ENSP00000309913.4:p.Arg237Trp
|
|
ENST00000349716.9:c.559C>T
|
ENSP00000337723.5:p.Arg187Trp
|
|
ENST00000405440.6:c.709C>T
|
ENSP00000384152.2:p.Arg237Trp
|
|
ENST00000526441.1:c.709C>T
|
ENSP00000433292.1:p.Arg237Trp
|
|
NM_000192.3:c.709C>T , LRG_670t1:c.709C>T
|
NP_000183.2:p.Arg237Trp
|
|
NM_080717.2:c.559C>T
|
NP_542448.1:p.Arg187Trp
|
|
NM_181486.2:c.709C>T
|
NP_852259.1:p.Arg237Trp
|
|
XM_017019912.1:c.757C>T
|
XP_016875401.1:p.Arg253Trp
|
|
NM_080717.3:c.559C>T
|
NP_542448.1:p.Arg187Trp
|
|
NM_181486.4:c.709C>T
MANE Select
|
NP_852259.1:p.Arg237Trp
|
|
NM_080717.4:c.559C>T
|
NP_542448.1:p.Arg187Trp
|
|