ENST00000610761.2:c.3238-134C>T
MANE Select
|
ENSP00000481780.1:n.3238-134C>T
|
|
ENST00000673691.1:c.3259-134C>T
|
ENSP00000501096.1:n.3259-134C>T
|
|
ENST00000250894.8:c.3235-134C>T
|
ENSP00000250894.4:n.3235-134C>T
|
|
ENST00000356010.9:c.3217-134C>T
|
ENSP00000348290.5:n.3217-134C>T
|
|
ENST00000564868.1:n.141-134C>T
|
|
|
ENST00000566064.1:n.164C>T
|
|
|
ENST00000610761.1:c.3238-134C>T
|
ENSP00000481780.1:n.3238-134C>T
|
|
NM_001040439.1:c.3217-134C>T
|
NP_001035529.1:n.3217-134C>T
|
|
NM_015133.3:c.3235-134C>T
|
NP_055948.2:n.3235-134C>T
|
|
XM_005255187.1:c.3238-134C>T
|
XP_005255244.1:n.3238-134C>T
|
|
XM_005255190.1:c.3193-134C>T
|
XP_005255247.1:n.3193-134C>T
|
|
XM_006720869.1:c.2476-134C>T
|
XP_006720932.1:n.2476-134C>T
|
|
XM_011522429.1:c.3262-134C>T
|
XP_011520731.1:n.3262-134C>T
|
|
XM_011522430.1:c.3244-134C>T
|
XP_011520732.1:n.3244-134C>T
|
|
XM_011522431.1:c.3235-134C>T
|
XP_011520733.1:n.3235-134C>T
|
|
XM_011522432.1:c.3217-134C>T
|
XP_011520734.1:n.3217-134C>T
|
|
XM_011522433.1:c.2758-134C>T
|
XP_011520735.1:n.2758-134C>T
|
|
NM_001318852.1:c.3238-134C>T
|
NP_001305781.1:n.3238-134C>T
|
|
NM_015133.4:c.3235-134C>T
|
NP_055948.2:n.3235-134C>T
|
|
XM_005255190.2:c.3193-134C>T
|
XP_005255247.1:n.3193-134C>T
|
|
XM_011522429.2:c.3262-134C>T
|
XP_011520731.1:n.3262-134C>T
|
|
XM_011522430.2:c.3244-134C>T
|
XP_011520732.1:n.3244-134C>T
|
|
XM_024450201.1:c.3262-134C>T
|
XP_024305969.1:n.3262-134C>T
|
|
XM_024450202.1:c.3244-134C>T
|
XP_024305970.1:n.3244-134C>T
|
|
XM_024450203.1:c.3238-134C>T
|
XP_024305971.1:n.3238-134C>T
|
|
XM_024450204.1:c.3235-134C>T
|
XP_024305972.1:n.3235-134C>T
|
|
XM_024450205.1:c.3235-134C>T
|
XP_024305973.1:n.3235-134C>T
|
|
XM_024450206.1:c.3220-134C>T
|
XP_024305974.1:n.3220-134C>T
|
|
XM_024450207.1:c.3217-134C>T
|
XP_024305975.1:n.3217-134C>T
|
|
XM_024450208.1:c.3211-134C>T
|
XP_024305976.1:n.3211-134C>T
|
|
XM_024450209.1:c.2764-134C>T
|
XP_024305977.1:n.2764-134C>T
|
|
XM_024450210.1:c.2758-134C>T
|
XP_024305978.1:n.2758-134C>T
|
|
XM_024450211.1:c.2476-134C>T
|
XP_024305979.1:n.2476-134C>T
|
|
NM_001040439.2:c.3217-134C>T
|
NP_001035529.1:n.3217-134C>T
|
|
NM_015133.5:c.3235-134C>T
|
NP_055948.2:n.3235-134C>T
|
|
NM_001318852.2:c.3238-134C>T
MANE Select
|
NP_001305781.1:n.3238-134C>T
|
|