ENST00000265631.10:c.1676A>T
MANE Select
|
ENSP00000265631.6:p.Tyr559Phe
|
|
ENST00000265631.9:c.1676A>T
|
ENSP00000265631.5:p.Tyr559Phe
|
|
ENST00000416240.6:c.1679A>T
|
ENSP00000400101.2:p.Tyr560Phe
|
|
ENST00000494085.1:n.86A>T
|
|
|
NM_001160210.1:c.1679A>T
|
NP_001153682.1:p.Tyr560Phe
|
|
NM_014251.2:c.1676A>T
|
NP_055066.1:p.Tyr559Phe
|
|
NR_027662.1:n.1751A>T
|
|
|
XM_006715831.2:c.1709A>T
|
XP_006715894.1:p.Tyr570Phe
|
|
XM_011515728.1:c.824A>T
|
XP_011514030.1:p.Tyr275Phe
|
|
XM_006715831.4:c.1709A>T
|
XP_006715894.1:p.Tyr570Phe
|
|
XM_017011663.1:c.1667A>T
|
XP_016867152.1:p.Tyr556Phe
|
|
XM_017011664.2:c.824A>T
|
XP_016867153.1:p.Tyr275Phe
|
|
XM_017011665.1:c.824A>T
|
XP_016867154.1:p.Tyr275Phe
|
|
XR_001744525.2:n.1922A>T
|
|
|
XR_002956405.1:n.2480A>T
|
|
|
NM_014251.3:c.1676A>T
MANE Select
|
NP_055066.1:p.Tyr559Phe
|
|
NR_027662.2:n.1702A>T
|
|
|
NM_001160210.2:c.1679A>T
|
NP_001153682.1:p.Tyr560Phe
|
|