ENST00000700518.1:c.9787C>T
|
ENSP00000515025.1:p.Leu3263Phe
|
|
ENST00000700519.1:c.9778C>T
|
ENSP00000515026.1:p.Leu3260Phe
|
|
ENST00000421745.7:c.9838C>T
MANE Select
|
ENSP00000393596.2:p.Leu3280Phe
|
|
ENST00000648282.1:c.9624C>T
|
|
|
ENST00000421745.6:c.9838C>T
|
ENSP00000393596.2:p.Leu3280Phe
|
|
NM_016252.3:c.9838C>T
|
NP_057336.3:p.Leu3280Phe
|
|
XM_005264449.3:c.9919C>T
|
XP_005264506.2:p.Leu3307Phe
|
|
XM_005264450.3:c.9907C>T
|
XP_005264507.2:p.Leu3303Phe
|
|
XM_005264451.3:c.9892C>T
|
XP_005264508.2:p.Leu3298Phe
|
|
XM_005264452.3:c.9877C>T
|
XP_005264509.2:p.Leu3293Phe
|
|
XM_005264453.3:c.9850C>T
|
XP_005264510.2:p.Leu3284Phe
|
|
XM_005264454.3:c.9919C>T
|
XP_005264511.2:p.Leu3307Phe
|
|
XM_005264455.3:c.9787C>T
|
XP_005264512.2:p.Leu3263Phe
|
|
XM_006712054.2:c.9901C>T
|
XP_006712117.1:p.Leu3301Phe
|
|
XM_006712055.2:c.9919C>T
|
XP_006712118.1:p.Leu3307Phe
|
|
XM_006712056.2:c.9820C>T
|
XP_006712119.1:p.Leu3274Phe
|
|
XM_006712057.2:c.9703C>T
|
XP_006712120.1:p.Leu3235Phe
|
|
XM_011533003.1:c.9604C>T
|
XP_011531305.1:p.Leu3202Phe
|
|
XM_011533004.1:c.9919C>T
|
XP_011531306.1:p.Leu3307Phe
|
|
XM_011533005.1:c.9919C>T
|
XP_011531307.1:p.Leu3307Phe
|
|
XR_244950.3:n.9949C>T
|
|
|
XM_005264449.4:c.9919C>T
|
XP_005264506.2:p.Leu3307Phe
|
|
XM_005264450.4:c.9907C>T
|
XP_005264507.2:p.Leu3303Phe
|
|
XM_005264451.4:c.9892C>T
|
XP_005264508.2:p.Leu3298Phe
|
|
XM_005264452.4:c.9877C>T
|
XP_005264509.2:p.Leu3293Phe
|
|
XM_005264453.4:c.9850C>T
|
XP_005264510.2:p.Leu3284Phe
|
|
XM_005264454.5:c.9919C>T
|
XP_005264511.2:p.Leu3307Phe
|
|
XM_005264455.4:c.9787C>T
|
XP_005264512.2:p.Leu3263Phe
|
|
XM_006712054.3:c.9901C>T
|
XP_006712117.1:p.Leu3301Phe
|
|
XM_006712055.3:c.9919C>T
|
XP_006712118.1:p.Leu3307Phe
|
|
XM_006712056.3:c.9820C>T
|
XP_006712119.1:p.Leu3274Phe
|
|
XM_011533003.2:c.9604C>T
|
XP_011531305.1:p.Leu3202Phe
|
|
XM_011533005.2:c.9919C>T
|
XP_011531307.1:p.Leu3307Phe
|
|
XM_017004556.1:c.9901C>T
|
XP_016860045.1:p.Leu3301Phe
|
|
XM_017004557.1:c.9808C>T
|
XP_016860046.1:p.Leu3270Phe
|
|
XM_017004558.1:c.9778C>T
|
XP_016860047.1:p.Leu3260Phe
|
|
XM_017004559.1:c.9919C>T
|
XP_016860048.1:p.Leu3307Phe
|
|
XM_017004560.1:c.9901C>T
|
XP_016860049.1:p.Leu3301Phe
|
|
XR_001738858.2:n.10174C>T
|
|
|
XR_244950.4:n.10174C>T
|
|
|
NM_001378125.1:c.9835C>T
|
NP_001365054.1:p.Leu3279Phe
|
|
NM_016252.4:c.9838C>T
MANE Select
|
NP_057336.3:p.Leu3280Phe
|
|