ENST00000376199.7:c.964C>T
|
ENSP00000365372.2:p.Gln322Ter
|
|
ENST00000376207.10:c.1069C>T
MANE Select
|
ENSP00000365380.4:p.Gln357Ter
|
|
ENST00000455775.7:c.1138C>T
|
ENSP00000396415.3:p.Gln380Ter
|
|
ENST00000518685.6:c.988C>T
|
ENSP00000428952.2:p.Gln330Ter
|
|
ENST00000557224.6:c.964C>T
|
ENSP00000451208.1:p.Gln322Ter
|
|
ENST00000651307.1:c.992C>T
|
ENSP00000498454.1:p.Ala331Val
|
|
ENST00000376197.1:c.919C>T
|
ENSP00000365369.1:p.Gln307Ter
|
|
ENST00000376199.6:c.964C>T
|
ENSP00000365372.2:p.Gln322Ter
|
|
ENST00000376207.8:c.1069C>T
|
ENSP00000365380.4:p.Gln357Ter
|
|
ENST00000455775.6:c.1138C>T
|
ENSP00000396415.3:p.Gln380Ter
|
|
ENST00000518685.5:c.964C>T
|
ENSP00000428952.1:p.Gln322Ter
|
|
ENST00000557224.5:c.964C>T
|
ENSP00000451208.1:p.Gln322Ter
|
|
NM_001114377.1:c.964C>T
|
NP_001107849.1:p.Gln322Ter
|
|
NM_014009.3:c.1069C>T , LRG_62t1:c.1069C>T
|
NP_054728.2:p.Gln357Ter
|
|
XM_006724533.2:c.1138C>T
|
XP_006724596.2:p.Gln380Ter
|
|
XM_011543915.1:c.1288C>T
|
XP_011542217.1:p.Gln430Ter
|
|
XM_011543916.1:c.1288C>T
|
XP_011542218.1:p.Gln430Ter
|
|
XM_011543917.1:c.1087C>T
|
XP_011542219.1:p.Gln363Ter
|
|
XM_011543918.1:c.1324C>T
|
XP_011542220.1:p.Gln442Ter
|
|
XM_011543919.1:c.1288C>T
|
XP_011542221.1:p.Gln430Ter
|
|
XM_017029567.1:c.1015C>T
|
XP_016885056.1:p.Gln339Ter
|
|
NM_001114377.2:c.964C>T
|
NP_001107849.1:p.Gln322Ter
|
|
NM_014009.4:c.1069C>T
MANE Select
|
NP_054728.2:p.Gln357Ter
|
|