ENST00000326735.13:c.1325A>T
MANE Select
|
ENSP00000327214.8:p.Tyr442Phe
|
|
ENST00000326735.12:c.1325A>T
|
ENSP00000327214.8:p.Tyr442Phe
|
|
ENST00000341676.9:c.1310A>T
|
ENSP00000341115.5:p.Tyr437Phe
|
|
ENST00000452699.5:c.1310A>T
|
ENSP00000413307.1:p.Tyr437Phe
|
|
ENST00000463860.5:n.933A>T
|
|
|
ENST00000502860.1:n.353A>T
|
|
|
ENST00000503552.1:c.2A>T
|
ENSP00000421126.1:p.Tyr1Phe
|
|
ENST00000506174.5:c.467A>T
|
ENSP00000424393.1:p.Tyr156Phe
|
|
ENST00000509392.1:n.413A>T
|
|
|
ENST00000617114.4:c.353A>T
|
ENSP00000478781.1:p.Tyr118Phe
|
|
NM_001141973.2:c.1310A>T
|
NP_001135445.1:p.Tyr437Phe
|
|
NM_001141974.2:c.1310A>T
|
NP_001135446.1:p.Tyr437Phe
|
|
NM_022089.3:c.1325A>T
|
NP_071372.1:p.Tyr442Phe
|
|
XM_005245809.1:c.1325A>T
|
XP_005245866.1:p.Tyr442Phe
|
|
XM_005245810.1:c.1322A>T
|
XP_005245867.1:p.Tyr441Phe
|
|
XM_005245811.1:c.1310A>T
|
XP_005245868.1:p.Tyr437Phe
|
|
XM_005245812.1:c.1298A>T
|
XP_005245869.1:p.Tyr433Phe
|
|
XM_005245813.1:c.1325A>T
|
XP_005245870.1:p.Tyr442Phe
|
|
XM_005245815.1:c.1325A>T
|
XP_005245872.1:p.Tyr442Phe
|
|
XM_006710512.1:c.1307A>T
|
XP_006710575.1:p.Tyr436Phe
|
|
XM_006710513.1:c.1283A>T
|
XP_006710576.1:p.Tyr428Phe
|
|
XM_011541128.1:c.1325A>T
|
XP_011539430.1:p.Tyr442Phe
|
|
XM_011541129.1:c.1325A>T
|
XP_011539431.1:p.Tyr442Phe
|
|
XM_017000844.1:c.1325A>T
|
XP_016856333.1:p.Tyr442Phe
|
|
XM_017000845.1:c.1307A>T
|
XP_016856334.1:p.Tyr436Phe
|
|
XM_017000846.1:c.1283A>T
|
XP_016856335.1:p.Tyr428Phe
|
|
XM_017000847.1:c.1295A>T
|
XP_016856336.1:p.Tyr432Phe
|
|
XM_017000848.1:c.1325A>T
|
XP_016856337.1:p.Tyr442Phe
|
|
XM_017000849.1:c.1310A>T
|
XP_016856338.1:p.Tyr437Phe
|
|
XM_017000850.1:c.1325A>T
|
XP_016856339.1:p.Tyr442Phe
|
|
NM_022089.4:c.1325A>T
MANE Select
|
NP_071372.1:p.Tyr442Phe
|
|
NM_001141973.3:c.1310A>T
|
NP_001135445.1:p.Tyr437Phe
|
|
NM_001141974.3:c.1310A>T
|
NP_001135446.1:p.Tyr437Phe
|
|