ENST00000326735.13:c.3529G>C
MANE Select
|
ENSP00000327214.8:p.Gly1177Arg
|
|
ENST00000326735.12:c.3529G>C
|
ENSP00000327214.8:p.Gly1177Arg
|
|
ENST00000341676.9:c.3227G>C
|
ENSP00000341115.5:p.Arg1076Pro
|
|
ENST00000452699.5:c.3514G>C
|
ENSP00000413307.1:p.Gly1172Arg
|
|
ENST00000466561.1:n.1575G>C
|
|
|
ENST00000502418.1:c.947G>C
|
ENSP00000423065.1:p.Arg316Pro
|
|
NM_001141973.2:c.3514G>C
|
NP_001135445.1:p.Gly1172Arg
|
|
NM_001141974.2:c.3227G>C
|
NP_001135446.1:p.Arg1076Pro
|
|
NM_022089.3:c.3529G>C
|
NP_071372.1:p.Gly1177Arg
|
|
XM_005245809.1:c.3359G>C
|
XP_005245866.1:p.Arg1120Pro
|
|
XM_005245810.1:c.3356G>C
|
XP_005245867.1:p.Arg1119Pro
|
|
XM_005245811.1:c.3344G>C
|
XP_005245868.1:p.Arg1115Pro
|
|
XM_005245812.1:c.3332G>C
|
XP_005245869.1:p.Arg1111Pro
|
|
XM_005245813.1:c.3299G>C
|
XP_005245870.1:p.Arg1100Pro
|
|
XM_005245815.1:c.3242G>C
|
XP_005245872.1:p.Arg1081Pro
|
|
XM_006710512.1:c.3341G>C
|
XP_006710575.1:p.Arg1114Pro
|
|
XM_006710513.1:c.3317G>C
|
XP_006710576.1:p.Arg1106Pro
|
|
XM_011541128.1:c.3344G>C
|
XP_011539430.1:p.Arg1115Pro
|
|
XM_011541129.1:c.3152G>C
|
XP_011539431.1:p.Arg1051Pro
|
|
XM_017000844.1:c.3514G>C
|
XP_016856333.1:p.Gly1172Arg
|
|
XM_017000845.1:c.3511G>C
|
XP_016856334.1:p.Gly1171Arg
|
|
XM_017000846.1:c.3487G>C
|
XP_016856335.1:p.Gly1163Arg
|
|
XM_017000847.1:c.3484G>C
|
XP_016856336.1:p.Gly1162Arg
|
|
XM_017000848.1:c.3412G>C
|
XP_016856337.1:p.Gly1138Arg
|
|
XM_017000849.1:c.3397G>C
|
XP_016856338.1:p.Gly1133Arg
|
|
XM_017000850.1:c.3322G>C
|
XP_016856339.1:p.Gly1108Arg
|
|
NM_022089.4:c.3529G>C
MANE Select
|
NP_071372.1:p.Gly1177Arg
|
|
NM_001141973.3:c.3514G>C
|
NP_001135445.1:p.Gly1172Arg
|
|
NM_001141974.3:c.3227G>C
|
NP_001135446.1:p.Arg1076Pro
|
|