ENST00000583780.2:c.1412T>A
|
ENSP00000462041.2:p.Phe471Tyr
|
|
ENST00000316694.8:c.1412T>A
MANE Select
|
ENSP00000318868.3:p.Phe471Tyr
|
|
ENST00000316694.7:c.1412T>A
|
ENSP00000318868.3:p.Phe471Tyr
|
|
ENST00000352886.10:c.998T>A
|
ENSP00000345881.7:p.Phe333Tyr
|
|
ENST00000354098.7:c.1295T>A
|
ENSP00000318805.3:p.Phe432Tyr
|
|
ENST00000395684.5:n.1735T>A
|
|
|
ENST00000580002.5:c.*909T>A
|
ENSP00000462043.1:n.*909T>A
|
|
NM_001281786.1:c.998T>A
|
NP_001268715.1:p.Phe333Tyr
|
|
NM_004169.4:c.1412T>A
|
NP_004160.3:p.Phe471Tyr
|
|
NM_148918.2:c.1295T>A
|
NP_683718.1:p.Phe432Tyr
|
|
XM_005256767.2:c.1412T>A
|
XP_005256824.1:p.Phe471Tyr
|
|
XM_011523992.1:c.1172T>A
|
XP_011522294.1:p.Phe391Tyr
|
|
XM_005256767.3:c.1412T>A
|
XP_005256824.1:p.Phe471Tyr
|
|
XM_011523992.3:c.1172T>A
|
XP_011522294.1:p.Phe391Tyr
|
|
XM_017024957.1:c.1412T>A
|
XP_016880446.1:p.Phe471Tyr
|
|
XM_017024958.1:c.1295T>A
|
XP_016880447.1:p.Phe432Tyr
|
|
XM_024450887.1:c.1172T>A
|
XP_024306655.1:p.Phe391Tyr
|
|
XM_024450888.1:c.998T>A
|
XP_024306656.1:p.Phe333Tyr
|
|
XM_024450889.1:c.881T>A
|
XP_024306657.1:p.Phe294Tyr
|
|
XM_024450890.1:c.758T>A
|
XP_024306658.1:p.Phe253Tyr
|
|
NM_004169.5:c.1412T>A
MANE Select
|
NP_004160.3:p.Phe471Tyr
|
|
NM_001281786.2:c.998T>A
|
NP_001268715.1:p.Phe333Tyr
|
|
NM_148918.3:c.1295T>A
|
NP_683718.1:p.Phe432Tyr
|
|