ENST00000256084.8:c.2987A>T
MANE Select
|
ENSP00000256084.7:p.Tyr996Phe
|
|
ENST00000256084.7:c.2987A>T
|
ENSP00000256084.7:p.Tyr996Phe
|
|
ENST00000359874.7:c.3077A>T
|
ENSP00000352936.3:p.Tyr1026Phe
|
|
NM_001127698.1:c.3077A>T
|
NP_001121170.1:p.Tyr1026Phe
|
|
NM_006846.3:c.2987A>T , LRG_110t1:c.2987A>T
|
NP_006837.2:p.Tyr996Phe
|
|
XM_011537550.1:c.3020A>T
|
XP_011535852.1:p.Tyr1007Phe
|
|
XM_011537551.1:c.2993A>T
|
XP_011535853.1:p.Tyr998Phe
|
|
XM_011537551.2:c.2993A>T
|
XP_011535853.1:p.Tyr998Phe
|
|
NM_001127698.2:c.3077A>T
|
NP_001121170.1:p.Tyr1026Phe
|
|
NM_006846.4:c.2987A>T
MANE Select
|
NP_006837.2:p.Tyr996Phe
|
|